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IHC 007 ImmunoWash (10x) 1L

by Slmp, LLC

IHC 007 ImmunoWash (10x) 1L (ACR-024) is a Class I device made by Slmp, LLC, listed in FDA GUDID since 31 Mar 2025 (UDI-DI 00810170553622), 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 Number00810170553622 UDI-DI Date31 Mar 2025ListedStatusListed 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  • Withdrawn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
Ihc
Generic name
Immunohistochemistry wash buffer reagent IVD
Model / Ref / Catalog
007 ImmunoWash (10x) 1L, ACR-024
Primary DI / UDI-DI
00810170553622
FDA product code
PPM
GMDN term
Immunohistochemistry wash buffer reagent IVD
Device class
Class I
Regulation number
864.4010
GUDID distribution status
In Commercial Distribution

Similar devices

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

Other devices from Slmp, LLC

See all devices from Slmp, LLC →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)