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ProCure PCHTD410

by Twin Med, LLC

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 Number10840330701607 UDI-DI Date28 Apr 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  • Withdrawn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
ProCure
Generic Name
Defibrinated blood dressing
Model / Ref / Catalog
PCHTD410
Description
ProCure Healing Transparent Film Dressing 4"x10" - 10ea/bx 40bx/cs
Primary DI / UDI-DI
10840330701607
FDA Product Code
NAD
GMDN Term
Defibrinated blood dressing
Device Class
Class I
Regulation Number
878.4020
GUDID distribution status
In Commercial Distribution
Size
Length — 10 Centimeter
Width — 25 Centimeter

Other devices from Twin Med, LLC

See all devices from Twin Med, LLC →

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No