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DRAPE ARMOUR™ Drape Armour FPS

by Microtek Medical LLC 4 variants

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 Number00748426143467 UDI-DI Date25 Sep 2025ListedStatusListed 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  • Withdrawn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
Drape Armour™
Generic Name
Radiation shielding curtain
Model / Ref / Catalog
Drape Armour FPS, RBFPS103
Primary DI / UDI-DI
00748426143467
FDA Product Code
KPY
GMDN Term
Radiation shielding curtain
Device Class
Class I
Regulation Number
892.6500
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Other devices from Microtek Medical LLC

See all devices from Microtek Medical LLC →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

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