Skip to content

Medium half body incise drape wetlaid 127x140cm 60300273

by Nuline Limited

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 Number05060647232177 UDI-DI Date6 Oct 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  • Withdrawn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
Medium half body incise drape wetlaid 127x140cm
Generic Name
Ophthalmic surgical drape
Model / Reference
60300273
Primary DI / UDI-DI
05060647232177
FDA Product Code
HMT
GMDN Term
Ophthalmic surgical drape
Device Class
Class II
Regulation Number
878.4370
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Other devices from Nuline Limited

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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