← Back to catalogue

Cardiac Marker Control Tri-Lvl

FDA UDI

Class I (US FDA UDI)

by Cliniqa Corporation

Identity

Trade Name
CARDIAC MARKER CONTROL TRI-LVL FDA UDI
Generic Name
Multiple cardiac marker IVD, control FDA UDI
Device Name
CARDIAC MARKER CONTROL TRI-LVL (min-pack) FDA UDI
Model / Reference
91489 FDA UDI
Description
CARDIAC MARKER CONTROL TRI-LVL (min-pack) FDA UDI

Identifiers

Primary DI / UDI-DI
00817238010097 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple cardiac marker IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Cardiac Marker Control Tri-Lvl by Cliniqa Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cliniqa Corporation

Sources (1)

  • FDA UDI a45b815b-5d28-46dc-82d4-d8dca7db910a 34 fields · synced May 30, 2026