Kopans

Kopans Breast Lesion Localization Needle With Echotip

Registry build 21.09.26
3manufacturers in China registered for this device type
27catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Jiangsu (1), Guangdong (1), Zhejiang (1).

Chinese manufacturers registered for FDA product code MIJ
Manufacturer City Province Registered as Device types
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Shenzhen Xiazhifeng Electronic Co., Ltd. Shenzhen Guangdong Contract manufacturer 25
Ningbo Hysent Medical Technology Co., Ltd. Ningbo Zhejiang Manufacturer 13

Record

Regulatory record for Kopans
Listed by Cook Incorporated, United States
FDA product code MIJ
Device type Needle, Tumor Localization
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
Record revised 2023-09-18 (version 3)

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 Kopans
Catalogue number Size Status
G07370 In distribution
G09042 In distribution
G03795 In distribution
G26976 In distribution
G04271 In distribution
G03507 In distribution
G09985 In distribution
G02601 In distribution
G02554 In distribution
G02938 In distribution
G04053 In distribution
G09984 In distribution
G01193 In distribution
G12160 In distribution
G05862 In distribution
G02850 In distribution
G01258 In distribution
G02900 In distribution
G30182 In distribution
G04293 In distribution
G05346 In distribution
G26977 In distribution
G04343 In distribution
G02587 In distribution
G02586 In distribution
G04296 In distribution
G04060 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Medwire Medax Srl Unipersonale 22
Sinurep Medax Srl Unipersonale 9
ALM SET H.S. Hospital Service SPA 6
Cook Cook Incorporated 5
Tuflex Somatex Medical Technologies GmbH 4
Breast Needle Locator Remington Medical, Inc. 4
Q-Wire System Somatex Medical Technologies GmbH 3
Tuloc Premium Somatex Medical Technologies GmbH 3
Tuloc Somatex Medical Technologies GmbH 3
Tuflex Premium Somatex Medical Technologies GmbH 3
MRI Tuloc Somatex Medical Technologies GmbH 2
Duo System Stereo Somatex Medical Technologies GmbH 2

Showing 12 of 37. All products under Needle, Tumor Localization

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 Closed
2016-01-08 Class II Process control Product potentially exposed to body fluids during processing. Potential adverse events that may occur as a result of the foreign matter include blood borne pathogen transmission. However, the risk of transmission of blood borne pathogens i 134 2017-03-23

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