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Tissue-Tek® 5987

by Sakura Finetek USA, Inc

Tissue-Tek 5987 is a reagent grade alcohol solution IVD (FDA Class I; FDA product code PPM, General purpose reagent) made by Sakura Finetek USA, Inc, listed in FDA GUDID since 5 Sep 2020 (UDI-DI 00615233007285), 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 Number00615233007285 UDI-DI Date5 Sep 2020ListedStatusListed 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  • Withdrawn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
Tissue-Tek®
Generic name
Reagent grade alcohol solution IVD
Model / Ref / Catalog
5987
Primary DI / UDI-DI
00615233007285
FDA product code
PPM
GMDN term
Reagent grade alcohol solution IVD
Device class
Class I
Regulation number
864.4010
GUDID distribution status
In Commercial Distribution

Related devices

Category: Reagent grade alcohol solution IVD

Similar devices

Other devices filed under FDA product code PPM (General purpose reagent).

Other devices from Sakura Finetek USA, Inc

See all devices from Sakura Finetek USA, Inc →

Properties

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