Tuloc Premium

3 catalogue numbers from 271880, listed by Somatex Medical Technologies GmbH, Germany, under Needle, Tumor Localization. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue 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 Tuloc Premium
Listed by Somatex Medical Technologies GmbH, Germany
FDA product code MIJ
Device type Needle, Tumor Localization
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2021-10-28
Record revised 2026-07-03 (version 5)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Pack of 10

Catalogue Numbers

Catalogue numbers for Tuloc Premium
Catalogue number Size Status
271880 In distribution
271883 In distribution
271881 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Kopans Cook Incorporated 27
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 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
2021-02-03 Class II Device Design This recall has been initiated due to the risk of wire splintering after contact with a cautery device during the removal of a lesion. There is a potential risk that wire fragments are not removed during the procedure and stays inside the p 196 pieces 2022-01-13

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