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MIcroprotein Standard Kit

FDA UDI

Class II (US FDA UDI)

by Verichem Laboratories, Inc.

Identity

Trade Name
MIcroprotein Standard Kit FDA UDI
Generic Name
Total microprotein IVD, calibrator FDA UDI
Device Name
Calibrator / Calibration Verifier FDA UDI
Model / Reference
9480 FDA UDI
Description
Calibrator / Calibration Verifier FDA UDI

Identifiers

Primary DI / UDI-DI
00852553007193 FDA UDI
FDA Product Code
JIX FDA UDI
GMDN Term
Total microprotein IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

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 microprotein IVD, calibrator

MIcroprotein Standard Kit by Verichem Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total microprotein IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0010cc95-cd1f-4fc0-9bde-64ef55ac405a 34 fields · synced Jun 1, 2026