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Thrombin JMI - 5, 000 IU Epistaxis Kit NDC 60793-205-05

by Pfizer H.C.P. Corporation

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 Number10360793205059 UDI-DI Date17 Apr 2019ListedStatusListed 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  • Withdrawn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
Thrombin JMI - 5,000 IU Epistaxis Kit
Generic Name
General surgical procedure kit, medicated
Model / Reference
NDC 60793-205-05
Primary DI / UDI-DI
10360793205059
GMDN Term
General surgical procedure kit, medicated
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide
Size
Total Volume — 10 Milliliter

Related devices

Category: General surgical procedure kit, medicated

Other devices from Pfizer H.C.P. Corporation

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Combination Product
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No