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Pointe Creatine Kinase Reagent

FDA UDI

Class II (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Creatine Kinase Reagent FDA UDI
Generic Name
Total creatine kinase (CK) IVD, kit, enzyme spectrophotometry FDA UDI
Device Name
Pointe Creatine Kinase Reagent packaged for use on the Mindray BA800. 3 x 60ml R1, 3 x 15ml R2. For the quantitative determination of creatine kinase activity in serum. FDA UDI
Model / Reference
16-C7522-225 FDA UDI
Description
Pointe Creatine Kinase Reagent packaged for use on the Mindray BA800. 3 x 60ml R1, 3 x 15ml R2. For the quantitative determination of creatine kinase activity in serum. FDA UDI

Identifiers

Catalog Number
16-C7522-225 FDA UDI
Primary DI / UDI-DI
00811727016096 FDA UDI
510(k) Number
K972155 FDA UDI
FDA Product Code
CGS FDA UDI
GMDN Term
Total creatine kinase (CK) IVD, kit, enzyme spectrophotometry 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

Yes

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: Total creatine kinase (CK) IVD, kit, enzyme spectrophotometry

Pointe Creatine Kinase Reagent by Pointe Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total creatine kinase (CK) IVD, kit, enzyme spectrophotometry.

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 3060b649-ad9e-4a5f-959b-8c20fbeca55e 37 fields · synced May 30, 2026