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Total Protein (up)

FDA UDI

Class I (US FDA UDI)

by Randox Laboratories, Ltd.

Identity

Trade Name
TOTAL PROTEIN (UP) FDA UDI
Generic Name
Total protein IVD, kit, spectrophotometry FDA UDI
Device Name
For the quantitative in vitro determination of total protein in urine and C.S.F. FDA UDI
Model / Reference
UP1570 FDA UDI
Description
For the quantitative in vitro determination of total protein in urine and C.S.F. FDA UDI

Identifiers

Primary DI / UDI-DI
05055273206814 FDA UDI
FDA Product Code
JIR FDA UDI
GMDN Term
Total protein IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1645 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total protein IVD, kit, spectrophotometry

Total Protein (up) by Randox Laboratories, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total protein IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9b55802f-2e16-4368-851b-6c6e01799d8c 35 fields · synced May 30, 2026