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Medline-Microtek Protective Restraints

by Microtek Medical LLC 2 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 Number20748426263947 UDI-DI Date21 Jan 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  • Withdrawn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
Medline-Microtek
Generic Name
Limb/torso/head restraint, single-use
Model / Ref / Catalog
Protective Restraints, OPASN
Primary DI / UDI-DI
20748426263947
FDA Product Code
FMQ
GMDN Term
Limb/torso/head restraint, single-use
Device Class
Class I
Regulation Number
880.6760
GUDID distribution status
In Commercial Distribution

Other devices from Microtek Medical LLC

See all devices from Microtek Medical LLC →

Properties

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

Other properties (9)

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