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Powerpulse 71277005

by Smith & Nephew, Inc.

Powerpulse 71277005 is a Class II device made by Smith & Nephew, Inc., listed in FDA GUDID since 29 Aug 2015 (UDI-DI 03596010421302), 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 Number03596010421302 UDI-DI Date29 Aug 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  • Withdrawn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

Trade name
Powerpulse
Generic name
Surgical/orthopaedic lavage control unit
Model / Ref / Catalog
71277005
Primary DI / UDI-DI
03596010421302
FDA product code
FQH
GMDN term
Surgical/orthopaedic lavage control unit
Device class
Class II
Regulation number
880.5475
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical/orthopaedic lavage control unit

Similar devices

Other devices filed under FDA product code FQH (LAVAGE, JET).

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)