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Tissue-Tek® Glas™ 6419

by Sakura Finetek USA, Inc

Tissue-Tek® Glas™ 6419 is a Class I device made by Sakura Finetek USA, Inc, listed in FDA GUDID since 17 Mar 2020 (UDI-DI 00615233080653), 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 Number00615233080653 UDI-DI Date17 Mar 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  • Withdrawn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® Glas™
Generic name
Microscopy mounting medium IVD
Model / Ref / Catalog
6419
Primary DI / UDI-DI
00615233080653
FDA product code
KIM
GMDN term
Microscopy mounting medium IVD
Device class
Class I
Regulation number
864.3400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Microscopy mounting medium IVD

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Other devices filed under Microscopy mounting medium IVD.

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Properties

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