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Dimension® CKI/MBI CAL

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Dimension® CKI/MBI CAL FDA UDI
Generic Name
Creatine kinase myocardial isoenzyme (CKMB) IVD, calibrator FDA UDI
Device Name
CKI/MBI Calibrator, 2x2x2mL FDA UDI
Model / Reference
10464508 FDA UDI
Description
CKI/MBI Calibrator, 2x2x2mL FDA UDI

Identifiers

Catalog Number
DC32 FDA UDI
Primary DI / UDI-DI
00842768025549 FDA UDI
510(k) Number
K081731 FDA UDI
FDA Product Code
JIX FDA UDI
GMDN Term
Creatine kinase myocardial isoenzyme (CKMB) IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

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: Creatine kinase myocardial isoenzyme (CKMB) IVD, calibrator

Dimension® CKI/MBI CAL by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Creatine kinase myocardial isoenzyme (CKMB) IVD, calibrator.

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 cc937ed7-2ee2-478d-bdd4-fedf54ef9aa1 37 fields · synced Jun 8, 2026