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PeroxAbolish PXA969M

by Biocare Medical, LLC

PeroxAbolish PXA969M is a Class I device made by Biocare Medical, LLC, listed in FDA GUDID since 23 Sep 2022 (UDI-DI 00847627012432), 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 Number00847627012432 UDI-DI Date23 Sep 2022ListedStatusListed 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  • Withdrawn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
PeroxAbolish
Generic name
Immunohistochemistry endogenous enzyme blocking reagent IVD
Model / reference
PXA969M
Primary DI / UDI-DI
00847627012432
FDA product code
PPM
GMDN term
Immunohistochemistry endogenous enzyme blocking reagent IVD
Device class
Class I
Regulation number
864.4010
GUDID distribution status
In Commercial Distribution

Related devices

Category: Immunohistochemistry endogenous enzyme blocking reagent IVD

Similar devices

Other devices filed under FDA product code PPM (General Purpose Reagent).

Other devices from Biocare Medical, LLC

See all devices from Biocare Medical, LLC →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)