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Valve, Bleed Tail 7-00675

by Westmed, Inc.

Valve, Bleed Tail 7-00675 is a Class II device made by Westmed, Inc., listed in FDA GUDID since 30 Sep 2020 (UDI-DI 00709078010705), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00709078010705 UDI-DI Date30 Sep 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  • Withdrawn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
Valve, Bleed Tail
Generic name
Mechanical expiratory valve, single-use
Model / reference
7-00675
Primary DI / UDI-DI
00709078010705
FDA product code
CBP
GMDN term
Mechanical expiratory valve, single-use
Device class
Class II
Regulation number
868.5870
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code CBP (Valve, Non-Rebreathing).

Other devices from Westmed, Inc.

See all devices from Westmed, Inc. →

Properties

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