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Primed PM1-2120

by priMED Medical Products Inc

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 Number00842942012914 UDI-DI Date8 May 2026ListedStatusListed 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  • Withdrawn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
Primed
Generic Name
Sterilization packaging, single-use
Model / Reference
PM1-2120
Description
Fused Two Colour Sterilization Wrap, 20in x 20in, 51cm x 51cm, Purple+Blue.
Primary DI / UDI-DI
00842942012914
FDA Product Code
FRG
GMDN Term
Sterilization packaging, single-use
Device Class
Class II
Regulation Number
880.6850
GUDID distribution status
In Commercial Distribution

Other devices from Primed Medical Products Inc.

See all devices from Primed Medical Products Inc. →

Properties

  • Single Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

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