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PQ Autoclave Pouches (3-1/2" x 9") Blue Film (200) P23-0922

by Pearson Dental Supplies, 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD724P2309221 UDI-DI Date22 Aug 2016ListedStatusListed 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  • Withdrawn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
PQ Autoclave Pouches (3-1/2" x 9") Blue Film (200)
Generic Name
Sterilization packaging, single-use
Model / Reference
P23-0922
Primary DI / UDI-DI
D724P2309221
FDA Product Code
FRC
GMDN Term
Sterilization packaging, single-use
Device Class
Class II
Regulation Number
880.2800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sterilization packaging, single-use

Other devices from Pearson Dental Supplies, Inc.

See all devices from Pearson Dental Supplies, Inc. →

Properties

  • Single Use
  • Convenience Kit
  • Lot / Batch Number

Other properties (11)

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