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Medline GC090RSR

by Medline Industries, Inc.

Medline GC090RSR is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 13 May 2022 (UDI-DI 10888277371750), 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 Number10888277371750 UDI-DI Date13 May 2022ListedStatusListed 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  • Withdrawn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
Medline
Generic name
Paranasal sinus guide-catheter
Model / Ref / Catalog
GC090RSR
Primary DI / UDI-DI
10888277371750
FDA product code
KAM
GMDN term
Paranasal sinus guide-catheter
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Paranasal sinus guide-catheter

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)