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Novocastra™ D-SARC-A

by Leica Biosystems Newcastle, Limited

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05055331332622 UDI-DI Date6 Jul 2021ListedStatusListed 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  • Withdrawn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
Novocastra™
Generic Name
Assay development analyte-specific reagent IVD
Model / Ref / Catalog
D-SARC-A, NCL-d-SARC
Primary DI / UDI-DI
05055331332622
FDA Product Code
MVU
GMDN Term
Assay development analyte-specific reagent IVD
Device Class
Class I
Regulation Number
864.4020
GUDID distribution status
In Commercial Distribution

Other devices from Leica Biosystems Newcastle, Limited

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Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No