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Namic 0448720

by Navilyst Medical, Inc.

Namic 0448720 is a Class II device made by Navilyst Medical, Inc., listed in FDA GUDID since 20 Sep 2016 (UDI-DI H74904487200), 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 NumberH74904487200 UDI-DI Date20 Sep 2016ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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 / reference
0448720
Primary DI / UDI-DI
H74904487200
FDA product code
DQX
GMDN term
Torque manipulation device
Device class
Class II
Regulation number
870.1330
GUDID distribution status
In Commercial Distribution

Related devices

Category: Torque manipulation device

Similar devices

Other devices filed under FDA product code DQX (WIRE, GUIDE, CATHETER).

Other devices from Navilyst Medical, Inc.

See all devices from Navilyst Medical, Inc. →

Properties

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