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Fisherbrand 58676

by Fisher Scientific Company L.L.C.

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 Number00613647023082 UDI-DI Date7 Dec 2022ListedStatusListed 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  • Withdrawn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
Fisherbrand
Generic name
Tissue embedding mould IVD, single-use
Model / Ref / Catalog
58676, 22047277
Primary DI / UDI-DI
00613647023082
FDA product code
IDZ
GMDN term
Tissue embedding mould IVD, single-use
Device class
Class I
Regulation number
864.3010
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tissue embedding mould IVD, single-use

Other devices from Fisher Scientific Company L.L.C.

See all devices from Fisher Scientific Company L.L.C. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No