Identity
- Trade Name
- RapiTex® CRP FDA UDI
- Generic Name
- C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry FDA UDI
- Device Name
- Qualitative detection or semi-quantitative determination of C-reactive protein (CRP) in human serum FDA UDI
- Model / Reference
- 10446420 FDA UDI
- Description
- Qualitative detection or semi-quantitative determination of C-reactive protein (CRP) in human serum FDA UDI
Identifiers
- Catalog Number
- OUAX41 FDA UDI
- Primary DI / UDI-DI
- 00842768011085 FDA UDI
- 510(k) Number
- K903853 FDA UDI
- FDA Product Code
- DCN FDA UDI
- GMDN Term
- C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry 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
No
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
No
FDA UDI
Category: C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry
RapiTex® CRP by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Tinaquant CReactive Protein Gen3 — Roche Diagnostics Corp. · Class II
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- Yumizen C1200 CRP — Horiba Abx · Class II
Cleared under the same submission
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics Products Ltd
Sources (1)
- FDA UDI 86c0fffc-5cc2-43d4-ae14-e21b2f67cac8 37 fields · synced Jun 8, 2026