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Procedural Oxygen Mask 1003-MSA-MED

by Stryker Corp.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851438008232 UDI-DI Date6 Mar 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Procedural Oxygen Mask
Generic Name
Non-rebreathing oxygen face mask
Model / Ref / Catalog
1003-MSA-MED
Primary DI / UDI-DI
00851438008232
FDA Product Code
CCK
GMDN Term
Non-rebreathing oxygen face mask
Device Class
Class II
Regulation Number
868.1400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Non-rebreathing oxygen face mask

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No