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Legion 71442241

by Smith & Nephew, Inc.

Legion 71442241 is a Class II device made by Smith & Nephew, Inc., listed in FDA GUDID since 30 Mar 2017 (UDI-DI 00885556648216), 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 Number00885556648216 UDI-DI Date30 Mar 2017ListedStatusListed 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  • Withdrawn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

Trade name
Legion
Generic name
Bone-coring punch, single-use
Model / Ref / Catalog
71442241
Primary DI / UDI-DI
00885556648216
FDA product code
JWH, LRY
GMDN term
Bone-coring punch, single-use
Device class
Class II
Regulation number
888.3560, 878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone-coring punch, single-use

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)