Trocar

Transnasal, Tessier

Registry build 21.09.26
1manufacturer
1catalogue number

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code KBG
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Record

Regulatory record for Trocar
Listed by KLS-Martin L.P., United States
FDA product code KBG
Device type Trocar, Sinus
Device class Class 1
Regulation 21 CFR 874.4420
Establishment Specification developer, Manufacturer
Premarket notification Exempt
Record published 2018-09-26
Record revised 2024-08-26 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Trocar
Catalogue number Size Status
48-320-14-07 14.5 CM In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Level ONE Transbuccal KLS-Martin L.P. 31
Level ONE KLS-Martin L.P. 6
Jedmed Jedmed Instrument Company 4
V. Mueller Carefusion 2200, Inc. 1

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