Franseen

Franseen Lung Biopsy Needle

Registry build 21.09.26
5manufacturers in China registered for this device type
32catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Shanghai (1), Tianjin (1), Guangdong (1).

Chinese manufacturers registered for FDA product code MJG
Manufacturer City Province Registered as Device types
Shanghai KiNETIC Medical Co Ltd Shanghai Shanghai Contract manufacturer 19
Tianjin Newtrans Technology Development Tianjin Tianjin Exporter 11
Carbon (Shenzhen) Medical Device Co., Ltd. Shenzhen Guangdong Manufacturer 6
Ningbo Hicren Biotechnology Co., Ltd. Ningbo Zhejiang Manufacturer 5
Canyon Medical Inc. Nanjing Jiangsu Manufacturer 4

Record

Regulatory record for Franseen
Listed by Cook Incorporated, United States
FDA product code MJG
Device type Device, Percutaneous, Biopsy
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-10-02

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Store in dark, dry, cool place.

Catalogue Numbers

Catalogue numbers for Franseen
Catalogue number Size Status
G01799 In distribution
G04987 In distribution
G09212 In distribution
G02681 In distribution
G04986 In distribution
G02530 In distribution
G13586 In distribution
G01269 In distribution
G01275 In distribution
G01266 In distribution
G01272 In distribution
G04984 In distribution
G02529 In distribution
G01267 In distribution
G01486 In distribution
G01612 In distribution
G04941 In distribution
G01268 In distribution
G04171 In distribution
G04420 In distribution
G04939 In distribution
G05374 In distribution
G06318 In distribution
G08888 In distribution
G01274 In distribution
G01437 In distribution
G01432 In distribution
G04762 In distribution
G04940 In distribution
G01305 In distribution
G04257 In distribution
G04985 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Cardinal Health Cardinal Health 200, LLC 392
Cook Cook Incorporated 77
Intro M.D.L. S.R.L. 34
HandCut M.D.L. S.R.L. 22
Turner Cook Incorporated 15
Palium Needle M.D.L. S.R.L. 14
Primocut Pajunk Gmbh Medizintechnologie 13
FastCutP M.D.L. S.R.L. 10
Co-Axial Cannula Bundle Argon Medical Devices, Inc. 10
Medline Industries, Inc. Medline Industries, Inc. 10
Greene Cook Incorporated 10
PaliumNeedle M.D.L. S.R.L. 10

Showing 12 of 44. All products under Device, Percutaneous, Biopsy

Recalls

1 of these is 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
2024-03-01 Class II Under Investigation by firm Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility 6,178 units

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