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Medline 3152R

by Medline Industries, Inc.

Medline 3152R is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 29 Jan 2025 (UDI-DI 10888277325227), 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 Number10888277325227 UDI-DI Date29 Jan 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  • Withdrawn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
Medline
Generic name
Rigid endoscopic scissors, single-use
Model / Ref / Catalog
3152R
Primary DI / UDI-DI
10888277325227
FDA product code
NUJ
GMDN term
Rigid endoscopic scissors, single-use
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid endoscopic scissors, single-use

Similar devices

Other devices filed under FDA product code NUJ (Electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)