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Namic 90701242

by Navilyst Medical, Inc.

Namic 90701242 is a Class I device made by Navilyst Medical, Inc., listed in FDA GUDID since 19 Sep 2016 (UDI-DI H965907012420), 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 NumberH965907012420 UDI-DI Date19 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  • Withdrawn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
Invasive blood pressure monitoring tubing set
Model / reference
90701242
Primary DI / UDI-DI
H965907012420
FDA product code
DRI
GMDN term
Invasive blood pressure monitoring tubing set
Device class
Class I
Regulation number
870.2620
GUDID distribution status
In Commercial Distribution
Size
Length — 24 Inch

Related devices

Category: Invasive blood pressure monitoring tubing set

Other devices from Navilyst Medical, Inc.

See all devices from Navilyst Medical, Inc. →

Properties

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