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Roche CARDIAC Control Troponin T

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Roche CARDIAC Control Troponin T FDA UDI
Generic Name
Troponin T/Troponin I IVD, control FDA UDI
Model / Reference
11937553193 FDA UDI

Identifiers

Catalog Number
11937553193 FDA UDI
Primary DI / UDI-DI
04015630901234 FDA UDI
510(k) Number
K000784 FDA UDI
FDA Product Code
MMI FDA UDI
GMDN Term
Troponin T/Troponin I IVD, control 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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 T/Troponin I IVD, control

Roche CARDIAC Control Troponin T by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Troponin T/Troponin I IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 168b3a79-382a-474f-a53b-6e930c897466 35 fields · synced Jun 7, 2026