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Namic H74902470012

by Medline Industries, Inc.

Namic H74902470012 is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 26 Jul 2021 (UDI-DI 10193489078015), 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 Number10193489078015 UDI-DI Date26 Jul 2021ListedStatusListed 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  • Withdrawn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
Namic
Generic name
Torque manipulation device
Model / Ref / Catalog
H74902470012
Primary DI / UDI-DI
10193489078015
FDA product code
LOX
GMDN term
Torque manipulation device
Device class
Class II
Regulation number
870.5100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Torque manipulation device

Similar devices

Other devices filed under FDA product code LOX (Catheters, transluminal coronary angioplasty, percutaneous).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

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