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ichroma Reader

FDA UDI

Class II (US FDA UDI)

by Boditech Med, Inc.

Identity

Trade Name
ichroma Reader FDA UDI
Generic Name
C-reactive protein (CRP) IVD, kit, fluorescent immunoassay FDA UDI
Model / Reference
FPRR001 FDA UDI

Identifiers

Catalog Number
FPRR001 FDA UDI
Primary DI / UDI-DI
08806133010099 FDA UDI
FDA Product Code
DCN FDA UDI
GMDN Term
C-reactive protein (CRP) IVD, kit, fluorescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5270 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: C-reactive protein (CRP) IVD, kit, fluorescent immunoassay

ichroma Reader by Boditech Med, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as C-reactive protein (CRP) IVD, kit, fluorescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boditech Med, Inc.

Sources (1)

  • FDA UDI 500ac4fe-179e-484d-b8b0-fd17f7615191 34 fields · synced Jun 8, 2026