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PATHFAST cTnI-II

FDA UDIEUDAMED

Class II (US FDA UDI)

by Phc Corporation

Identity

Trade Name
PATHFAST cTnI-II FDA UDI
Generic Name
Troponin I IVD, kit, chemiluminescent immunoassay FDA UDI
Model / Reference
N/A FDA UDI

Identifiers

Primary DI / UDI-DI
04987595301131 FDA UDI
510(k) Number
K100130 FDA UDI
FDA Product Code
MMI FDA UDI
GMDN Term
Troponin I IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1215 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Troponin I IVD, kit, chemiluminescent immunoassay

PATHFAST cTnI-II by Phc Corporation — Class II — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Troponin I IVD, kit, chemiluminescent immunoassay.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Phc Corporation

Sources (2)

  • FDA UDI 1c2067bb-1e29-458e-942b-214fd18606d1 34 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced May 29, 2026