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Namic 60120059

by Navilyst Medical, Inc.

Namic 60120059 is a device made by Navilyst Medical, Inc., listed in FDA GUDID since 6 Aug 2018 (UDI-DI H965601200590), 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 NumberH965601200590 UDI-DI Date6 Aug 2018ListedStatusListed 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  • Withdrawn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
Angiography kit
Model / reference
60120059
Primary DI / UDI-DI
H965601200590
GMDN term
Angiography kit
GUDID distribution status
In Commercial Distribution

Related devices

Category: Angiography kit

Similar devices in this category

Other devices filed under Angiography kit.

Other devices from Navilyst Medical, Inc.

See all devices from Navilyst Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)