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Curad CUR136103RB

by Medline Industries, Inc.

Curad CUR136103RB is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 10 Jun 2025 (UDI-DI 00080196323794), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00080196323794 UDI-DI Date10 Jun 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Curad
Generic name
Eye patch, single-use
Model / Ref / Catalog
CUR136103RB
Primary DI / UDI-DI
00080196323794
FDA product code
KGX
GMDN term
Eye patch, single-use
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Eye patch

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Other devices filed under Eye patch.

Other devices from Medline Industries, Inc.

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Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)