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Creatinine Enzymatic

FDA UDI

Class II (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Creatinine Enzymatic FDA UDI
Generic Name
Creatinine IVD, kit, enzyme spectrophotometry FDA UDI
Device Name
For the quantitative enzymatic determination of creatinine in serum and urine. For In Vitro Diagnostic Use Only. FDA UDI
Model / Reference
12-C7548-162 FDA UDI
Description
For the quantitative enzymatic determination of creatinine in serum and urine. For In Vitro Diagnostic Use Only. FDA UDI

Identifiers

Catalog Number
12-C7548-162 FDA UDI
Primary DI / UDI-DI
00811727013507 FDA UDI
510(k) Number
K050283 FDA UDI
FDA Product Code
JFY FDA UDI
GMDN Term
Creatinine IVD, kit, enzyme spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1225 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: Creatinine IVD, kit, enzyme spectrophotometry

Creatinine Enzymatic by Pointe Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Creatinine 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 66a6d5bc-028d-4506-b2af-33f4c27ea1dd 37 fields · synced Jun 1, 2026