DR. Trussell

Kit Contains: C0R47, 12x100 Kii® BALLOON BLUNT TIP 6/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX CFS02, 5x100 Kii® SLEEVE ADVFIX 12/BX CA500, EPIX® UNIVERSAL CLIP APPLIER 3/BX CFR03, 5X100 Kii®…

Registry build 21.09.26

Kit Contains: C0R47, 12×100 Kii® BALLOON BLUNT TIP 6/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX CFS02, 5×100 Kii® SLEEVE ADVFIX 12/BX CA500, EPIX® UNIVERSAL CLIP APPLIER 3/BX CFR03, 5X100 Kii® OPT ADVFIX 6/BX CB030, 5mmx35cm EPIX® LAPA SCISSOR, 10/BX C4119, 32CM GRASPER REPOS CART, 10/BX

7manufacturers in China registered for this device type
1catalogue number
5recalls on this code

Who Else Makes It

Concentrated in Zhejiang (3), Anhui (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NWV
Manufacturer City Province Registered as Device types
Tonglu Qianyan Medtech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Hangzhou Endo Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 19
Anhui Shiyin Photoelectric Instrument Co., Ltd. Suzhou Anhui Specification developer 18
Tonglu Youshi Medical Instrument Co., Ltd. Tonglu Zhejiang Manufacturer 10
Anqing Changfan Medical Instrument Co., Ltd. Anqing Anhui Manufacturer 9
Suzhou SMH Co., Ltd. Suzhou Jiangsu Manufacturer 4
Hunan Handlike Minimally Invasive Surgery Co., Ltd. Changsha Hunan Manufacturer 3

Record

Regulatory record for DR. Trussell
Listed by Applied Medical Resources Corp., United States
FDA product code NWV
Device type Laparoscopic Accessories, Gynecologic
Device class Class 1
Regulation 21 CFR 884.1720
Establishment Contract manufacturer, Complaint-file establishment, Manufacturer
Record published 2015-10-16
Record revised 2024-08-07 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for DR. Trussell
Catalogue number Size Status
K2769 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Millennium Avalign Technologies, Inc. 201
AED National Advanced Endoscopy Devices, Inc. 173
Elmed Elmed, Inc. 36
Elite National Advanced Endoscopy Devices, Inc. 8
Elmed Incorporated Elmed, Inc. 7
AbGrab Lapovations, LLC 6
Integra® Jarit® Integra LifeSciences Production Corporation 5
Laparoscopic Accessories, Gynecologic Stryker Sustainability Solutions 5
Speedlock National Advanced Endoscopy Devices, Inc. 5
TroClear Mednium Corporation 5
Integra® Miltex® Integra LifeSciences Production Corporation 5
Eco Fit National Advanced Endoscopy Devices, Inc. 4

Showing 12 of 80. All products under Laparoscopic Accessories, Gynecologic

Recalls

5 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2020-03-17 Class II Under Investigation by firm There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage. 32,760 units 2022-02-17
2020-03-17 Class II Under Investigation by firm There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage. 12 units 2022-02-17
2020-03-17 Class II Under Investigation by firm There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage. 4320 units 2022-02-17
2020-03-17 Class II Under Investigation by firm There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage. 21 units 2022-02-17
2013-05-01 Class II Nonconforming Material/Component Applied Medical is conducting a voluntary recall on specific lot numbers of its Epix and Direct Drive Laparoscopic
Graspers. When the ratchet trigger is activated, if a great enough force is applied, there is a potential for the trigger
to
127,305 units 2014-02-06

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer