← Back to catalogue

Total Protein Kit (Biuret Method)

FDA UDI

Class II (US FDA UDI)

by Medicalsystem Biotechnology Co., Ltd.

Identity

Trade Name
Total Protein Kit (Biuret Method) FDA UDI
Generic Name
Total protein IVD, kit, enzyme spectrophotometry FDA UDI
Model / Reference
None FDA UDI

Identifiers

Primary DI / UDI-DI
06970291985192 FDA UDI
FDA Product Code
CEK FDA UDI
GMDN Term
Total protein IVD, kit, enzyme spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1635 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Total protein IVD, kit, enzyme spectrophotometry

Total Protein Kit (Biuret Method) by Medicalsystem Biotechnology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total protein IVD, kit, enzyme spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medicalsystem Biotechnology Co., Ltd.

Sources (1)

  • FDA UDI 318fd775-4dda-446b-a09f-9650c5dda6b2 32 fields · synced May 30, 2026