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Werewolf 72290144

by Smith & Nephew, Inc.

Werewolf 72290144 is a Class II device made by Smith & Nephew, Inc., listed in FDA GUDID since 7 Jan 2020 (UDI-DI 00885556739624), 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 Number00885556739624 UDI-DI Date7 Jan 2020ListedStatusListed 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  • Withdrawn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
Werewolf
Generic name
Electrosurgical system generator
Model / Ref / Catalog
72290144
Primary DI / UDI-DI
00885556739624
FDA product code
GEI
GMDN term
Electrosurgical system generator
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrosurgical system generator

Similar devices in this category

Other devices filed under Electrosurgical system generator.

Other devices from Smith & Nephew, Inc.

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Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)