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4181M

by Smith & Nephew, Inc.

4181M is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 22 Oct 2015 (UDI-DI 00885556606780), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885556606780 UDI-DI Date22 Oct 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Meniscus forceps
Model / Ref / Catalog
4181M
Primary DI / UDI-DI
00885556606780
FDA product code
NBH
GMDN term
Meniscus forceps
Device class
Class I
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Meniscus forceps

Similar devices

Also classified as Meniscus forceps.

Similar devices

Other devices filed under FDA product code NBH (ACCESSORIES,ARTHROSCOPIC).

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)