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Fresh Cells 76-0600R

by Diagnostic Hybrids, Inc.

Fresh Cells 76-0600R is a Class I device made by Diagnostic Hybrids, Inc., listed in FDA GUDID since 21 Sep 2018 (UDI-DI 30014613333845), 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 Number30014613333845 UDI-DI Date21 Sep 2018ListedStatusListed 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  • Withdrawn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
Fresh Cells
Generic name
Cell culture line IVD
Model / Ref / Catalog
76-0600R
Primary DI / UDI-DI
30014613333845
FDA product code
KIR
GMDN term
Cell culture line IVD
Device class
Class I
Regulation number
864.2280
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KIR (CELLS, ANIMAL AND HUMAN, CULTURED).

Other devices from Diagnostic Hybrids, Inc.

See all devices from Diagnostic Hybrids, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)