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Medline 7210076RH

by Medline Industries, Inc.

Medline 7210076RH is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 8 Apr 2022 (UDI-DI 10888277385160), 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 Number10888277385160 UDI-DI Date8 Apr 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  • Withdrawn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
Suture cutter, single-use
Model / Ref / Catalog
7210076RH
Primary DI / UDI-DI
10888277385160
FDA product code
GDF
GMDN term
Suture cutter, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Suture cutter, single-use

Similar devices

Other devices filed under FDA product code GDF (GUIDE, NEEDLE, SURGICAL).

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)