News Updates

Robotic versus laparoscopic ventral hernia repair: multicenter, blinded randomized controlled trial

Objective To determine whether robotic ventral hernia repair is associated with fewer days in the hospital 90 days after surgery compared with laparoscopic repair.

2022-9-17 Take you through the disinfection method of middle ear scissors

         We all know that scissors, while they may be unattractive, are versatile. When tools such as knives and shovels fail, scissors can easily solve the problem. The middle ear scissors is one of them. Below, we will share the disinfection method of the middle ear scissors and understand it together.          During the procedure, it may also be necessary to use the middle ear to cut off the skin, pterygium, blood tendons, etc., to make the procedure go more smoothly. Middle ear clippers are made of specialized materials and shaped to suit the needs of the operation, so you should know that they can be different from normal middle ear clippers and need to be sterilized before use. The tools of life. To disinfect, soak middle ear scissors and forceps with a new diluted fungicide. The disinfectant is usually changed weekly. Then you can sterilize it with alcohol. Use Dharma to disinfect, GENERAL disinfectant HAS 7 days to change have 14 days to see specific varieties. In addition to these words can also do is high pressure steam sterilization, when the steam pressure reaches 104.0 ~ 137.3kPa, the temperature can reach 121 ~ 126℃. At this temperature for 30 minutes, it kills all microorganisms, including the more resistant bacterial spores. And then the new celamide 0.1% skin, mucous membrane, blister. Neogelamine 0.1% 1000ml, 5G medical sodium nitrite, used for long-term immersion of middle ear scissors. It is recommended not to mix with soap, iodine, and alkalis.            In addition, when disinfecting the middle ear clippers, the personnel inspecting and packing the area should first check for cleanliness by visual inspection or careful observation under a high-power magnifying glass with a light source. The surface of the middle ear scissors and every inch and gap of the joints and blades are free from stains and rust. In addition, we recommend ensuring good function of the middle ear scissors. Whether the blade is sharp, whether the joint is stuck, and whether the shear performance meets the standard, employees need to make accurate judgments through strict functional inspection and test methods as well as the sharp feel. In conclusion, we need to know that middle ear scissors are the surgeon's key weapon on the battlefield. If convergence and blockage occur, it may first affect the hand feeling of the owner, may also affect the operation effect, and may even lead to the failure of the operation. Of course, there is another way. For example, boil the water for three to five minutes, then drop the knife and middle ear scissors into the boiling water. Generally, bacteria can be killed by boiling for 15 minutes, but it takes 60 minutes for spores to become effective. Of course, dipping the instrument in saline is not allowed here either, as exposure to saline can cause pitting and corrosion. When soaking with multi-enzyme detergent, the concentration and soaking time specified in the instruction manual must be strictly followed.        The content of the above article is a few methods of disinfection of the middle ear scissors told about by friends, hoping to bring help for everyone!    

2022-8-10 What are the characteristics of the urethral dilator?

              Along with the advance of science and technology, the machine in use is also more and more get the recognition from all walks of life, and with the help of a machine can complete people finish or too time consuming, so the urethra dilator as important equipment, daily maintenance and maintenance is also very important, not only can reduce the pain of patients, can ensure the normal operation of the operation. Here we will introduce the characteristics of urethral dilator in detail, and learn about it together!              The main feature of the urethral dilator is that the urethral dilator includes a handle part, a curved part and a straight tube part. So here what we call the straight tube department connected to one department, the other end of the connection handle department surgery to daily operation, and then its handle department is mainly including straight face, and to connect the transition surface and curved surface, and the handle on this and straight pipe and the bend is an integral forming, and it is also equipped with interface, the connection of the transition surface The distal end of the bent part of the urethral dilator is in the form of rounded head structure, which is convenient to use in the operation. And there is an interface that needs to be used, so this interface is flared, and it is communicated with the hollow channel. And in the urethral dilator the junction between the handle and the straight tube forms a ladder structure.               In use, we use the urethral dilator to first detect whether the urethra is relatively narrow, and the extent of the narrow part and the whole. The urethral dilator is mainly to use the urethral rigid probe, and through the exploration of the urethra, as well as mechanical massage expansion, which can enhance the local blood circulation, so as to promote the softening and infiltration and absorption of scar tissue. Then in this process, we should know whether there are stones or foreign bodies in the urethra. In addition, I use urethral dilator during surgery to prevent and treat urethral inflammation, injury, and stenosis after surgery. Especially in women with distal urethral constriction with varying degrees of dysuria, then a large urethral probe can be used to dilate. And contracture obstruction throughout the neck of the bladder. And the use of urethral dilator this technique has become a very common surgical means of urology.            The above is the urethral dilator related knowledge introduction, I hope you will be helpful after reading.                          

Country SFDA issued a document: 22 kinds of instruments may be prohibited from commissioned production

According to the regulations on the supervision and administration of medical devices, China The SFDA organized and adjusted the catalogue of high-risk implantable medical devices prohibited from commissioned production to form the catalogue of medical devices prohibited from commissioned production (Draft for comments) (hereinafter referred to as the catalogue). On November 19, the public solicited opinions. The adjusted catalogue of high-risk implantable medical devices prohibited from commissioned production includes the following three types and 22 kinds of medical devices: 1、 Partially active implantable medical devices 1. Implantable pacemaker (12-01-01) 2. Implantable cardioverter defibrillator (12-01-02) 3. Implantable cardiac contractility regulator (12-04-01) 4. Implantable circulatory AIDS (12-04-02) 2、 Partially passive implanted medical devices 1. Sports injury soft tissue replacement implant (allogeneic tissue) (13-02-02) 2. Acrylic resin bone cement (13-05-01) 3. Allogeneic bone repair materials (13-05-03) 4. Dural patch (13-06-04) 5. Aneurysm clip (13-06-05) 6. Intracranial stent system (13-06-06) 7. Intracranial embolization instrument (13-06-07) 8. Intracranial coil system (13-06-08) 9. Flow guiding device for intracranial aneurysms (13-06-11) 10. Cardiovascular implants (excluding peripheral vascular stents) (13-07) 11. Shaping filling material (13-09-01) 12. Injection filler for plastic surgery (13-09-02) 13. Breast implants (13-09-03) 14. Tissue engineering scaffold materials (13-10) 3、 Other 1. Absorbable surgical anti adhesion dressing (14-08-02) 2. Tissue engineered biological amniotic membrane (16-07-09) 3. Corneal stromal slice (16-07-10) 4. Vaginal patch and pelvic floor patch (18-04-02) Note: the number in brackets after the product name is the category code of medical device classification catalogue (2017 Edition). Compared with the 2014 version, the adjusted catalogue will increase the number of medical devices prohibited from commissioned production to 22 and be more detailed. For example, the item of "plastic implants (agents)" listed in the original catalogue is subdivided into plastic filling materials, plastic injection fillers, breast implants and tissue engineering scaffold materials in the new catalogue. The catalogue of prohibited commissioned production of medical devices (Exposure Draft) is a timely adjustment under the continuous improvement of laws, regulations and standards and the continuous development of science and technology. The implementation of the catalogue will play a beneficial role in reducing adverse events of related products and ensuring product * * in the future.

Medical bone needle, Kirschner wire, steel needle, bone traction needle, titanium alloy + stainless steel, made by Dabang

Country The Home Drug Administration named: these medical devices are unqualified!

The notice shows that in order to strengthen the supervision and management of medical devices and ensure the quality of medical devices * * is effective The National Drug Administration organized the product quality supervision and sampling inspection of five varieties such as intervertebral fusion cage and semiconductor laser treatment machine, and a total of 12 batches (sets) of products did not meet the standards. The details are as follows: 1、 Medical device products whose sampled items do not meet the standards （1） Two batches of interbody fusion cage: produced by Dezhou Jinyue Medical Instrument Co., Ltd., the surface roughness involved does not meet the standard. （2） 1 set of semiconductor laser treatment machine: produced by Cao group, Inc. Siro group, the marking involved does not meet the standard provisions. （3） One carbon dioxide laser treatment machine: produced by Wuhan jinlaite optoelectronics Co., Ltd., which involves the external marking of equipment or equipment components, and the accuracy and marking of controller and instrument do not meet the standard provisions. （4） 1 set of ultrasonic equipment produced by Weihai Technology Co., Ltd. or external imaging equipment that does not meet the requirements of Weihai Technology Co., Ltd. （5） 7 operation shadowless lamps: produced by Changzhou Meiya medical Lighting Co., Ltd., Hebei Yi'an Aomei Medical Equipment Co., Ltd., Hengzhi medical equipment (Shanghai) Co., Ltd., Shandong KANGYI Medical Equipment Co., Ltd., Shandong xinyuchen Medical Equipment Group Co., Ltd., Shandong Xinhua Medical Equipment Co., Ltd. and Shanghai Jishun medical equipment manufacturing Co., Ltd., involving protective grounding impedance, central illumination The single shutter illumination measurement and total irradiance do not meet the standard requirements. The above sampling inspection does not meet the standard provisions. See the annex for the specific conditions of products. 2、 For the above products found in the sampling inspection that do not meet the standards and regulations, China will be punished The drug administration has asked the provincial drug administration where the enterprise is located to make administrative decisions in time and publish them to the society in accordance with the requirements of the regulations on the supervision and administration of medical devices, the measures for the supervision and administration of the production of medical devices and the measures for the administration of the recall of medical devices. The provincial drug supervision and administration department shall urge enterprises to conduct risk assessment on products that do not meet the standards, determine the recall level according to the severity of medical device defects, take the initiative to recall products and disclose the recall information; Urge enterprises to find out the causes of unqualified products as soon as possible, formulate rectification measures and rectify them in place on schedule.

2021.5.13-16 Our company participated in the 84th China International Medical Equipment Fair (CMEF Autumn Shanghai)

2021.5.13-16 Our company participated in the 84th China International Medical Equipment Fair (CMEF Autumn Shanghai)

Another Internet giant enters the medical device market, "co-builder" or "spoiler"?

Internet giants are scrambling for medical devices. Recently, Tiktok e-commerce has issued a public notice on the new [medical devices] category management specification, integrating the medical devices under various categories to make the medical devices into a separate category. This means that Tiktok is officially working in the field of medical devices. Previously, Internet giants, including Tencent, Alibaba, Baidu, meituan, Kwai, Xiaomi, pinduoduo and so on, have laid out medical devices: they either take shares in medical device enterprises by means of investment, or lay out their own layout in person, and invest in people, money and investment channels, thus marking their own base in the medical device Jianghu. To this end, Shao Qing, the founder and CEO of Beijing Pharmaceutical enabling technology Co., Ltd., was interviewed by [medical observer]. Shao Qing expressed his views on this trend: Q: Internet giants are laying out medical devices, which reflects the giants' consideration? Is the entry of Internet giants a "co builder" or a "troublemaker" in the development of the medical device industry? A: Medical devices, like drugs, are a category with relatively high gross profit margin, and capital pursues profit. Therefore, in the future, all platforms will make medicine and medical devices, but selling drugs may be more difficult than selling health products and medical devices. The entry of Internet giants is not only a "co builder" but also a "troublemaker" on the development of the medical device industry. They are "troublemakers" in the existing market and will seize part of the market; At the same time, they are also "co builders", providing better consumption scenes for product sales, such as live broadcasting, so as to better promote products.

2020.10.19-22 Our company participated in the 83rd China International Medical Equipment Fair (CMEF Autumn Shanghai)

2020.10.19-22 Our company participated in the 83rd China International Medical Equipment Fair (CMEF Autumn Shanghai)