Coatest Heparin

FDA UDI

Class II (US FDA UDI)

by Instrumentation Laboratory Company

Identity

Trade Name: Coatest Heparin FDA UDI
Generic Name: Heparin anti-Xa IVD, kit, chromogenic FDA UDI
Device Name: Coatest Heparin FDA UDI
Model / Reference: 25 5539 63 FDA UDI
Description: Coatest Heparin FDA UDI

Identifiers

Catalog Number: 25 5539 63 FDA UDI
Primary DI / UDI-DI: 08426950088196 FDA UDI
510(k) Number: K833891 FDA UDI
FDA Product Code: KFF FDA UDI
GMDN Term: Heparin anti-Xa IVD, kit, chromogenic FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 864.7525 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Heparin anti-Xa IVD, kit, chromogenic

Coatest Heparin by Instrumentation Laboratory Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Heparin anti-Xa IVD, kit, chromogenic.

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LR-ACT — MEDTRONIC, INC. · Class II
RACT — MEDTRONIC, INC. · Class II
ACTICHROME HEPARIN (ANTI-FXA) — Biomedica ADI Inc. · Class II
STA® - Liquid Anti-Xa 4 — DIAGNOSTICA STAGO, INC. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Instrumentation Laboratory Company

Sources (1)

FDA UDI 23b502af-4621-4c70-a6db-6cbf64746577 37 fields · synced May 30, 2026