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CRP Calibrator Kit

FDA UDI

Class II (US FDA UDI)

by Medica Corp.

Identity

Trade Name
CRP Calibrator Kit FDA UDI
Generic Name
C-reactive protein (CRP) IVD, calibrator FDA UDI
Device Name
CRP Calibrator Kit for use with EasyRA Analyzer FDA UDI
Model / Reference
10659 FDA UDI
Description
CRP Calibrator Kit for use with EasyRA Analyzer FDA UDI

Identifiers

Catalog Number
10659 FDA UDI
Primary DI / UDI-DI
00386100001803 FDA UDI
510(k) Number
K130080 FDA UDI
FDA Product Code
JIT FDA UDI
GMDN Term
C-reactive protein (CRP) 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: C-reactive protein (CRP) IVD, calibrator

CRP Calibrator Kit by Medica Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as C-reactive protein (CRP) IVD, calibrator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medica Corp.

Sources (1)

  • FDA UDI 089563df-3b64-47a9-8f2d-66d9a42cf4fa 37 fields · synced May 30, 2026