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CoreDish M970-D12LGI

by Simport Scientific Inc.

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 Number20667243012142 UDI-DI Date15 Jun 2026ListedStatusListed 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  • Withdrawn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
CoreDish
Generic Name
General tissue specimen container IVD, fixative/saline
Model / Reference
M970-D12LGI
Primary DI / UDI-DI
20667243012142
GMDN Term
General tissue specimen container IVD, fixative/saline
GUDID distribution status
In Commercial Distribution

Other devices from Simport Scientific Inc.

See all devices from Simport Scientific Inc. →

Properties

  • Single Use
  • Convenience Kit

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No