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Total Protein

FDA UDI

Class II (US FDA UDI)

by Sekisui Diagnostics, LLC

Identity

Trade Name
TOTAL PROTEIN FDA UDI
Generic Name
Total protein IVD, kit, spectrophotometry FDA UDI
Model / Reference
200-55 FDA UDI

Identifiers

Catalog Number
200-55 FDA UDI
Primary DI / UDI-DI
00628063400874 FDA UDI
510(k) Number
K843028 FDA UDI
FDA Product Code
CEK FDA UDI
GMDN Term
Total protein IVD, kit, 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

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 protein IVD, kit, spectrophotometry

Total Protein by Sekisui Diagnostics, LLC — Class II — 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 62e3a2a7-2c40-49ab-b10f-6dcf48ad3e82 34 fields · synced Jun 9, 2026