Identity
- Trade Name
- ADVIA Centaur® CpS FDA UDI
- Generic Name
- C-peptide IVD, kit, chemiluminescent immunoassay FDA UDI
- Device Name
- C-Peptide - CENTAUR - RGT - 100 tests FDA UDI
- Model / Reference
- 10310448 FDA UDI
- Description
- C-Peptide - CENTAUR - RGT - 100 tests FDA UDI
Identifiers
- Catalog Number
- 129026 FDA UDI
- Primary DI / UDI-DI
- 00630414464053 FDA UDI
- FDA Product Code
- JKD FDA UDI
- GMDN Term
- C-peptide IVD, kit, chemiluminescent immunoassay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1135 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
Yes
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-peptide IVD, kit, chemiluminescent immunoassay
ADVIA Centaur® CpS by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- C-Peptide ELISA — DRG International, Inc. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI 7f84d19e-2583-4461-b3c6-cd77992fc549 36 fields · synced May 31, 2026