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IMMULITE® Systems AFP Calibration Verification Material
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- IMMULITE® Systems AFP Calibration Verification Material FDA UDI
- Generic Name
- Alpha-fetoprotein (AFP) IVD, control FDA UDI
- Device Name
- AFP CVM - IMMULITE - CONS FDA UDI
- Model / Reference
- 10373681 FDA UDI
- Description
- AFP CVM - IMMULITE - CONS FDA UDI
Identifiers
- Catalog Number
- LAPCVM FDA UDI
- Primary DI / UDI-DI
- 00630414971148 FDA UDI
- 510(k) Number
- K132739 FDA UDI
- FDA Product Code
- JJX FDA UDI
- GMDN Term
- Alpha-fetoprotein (AFP) IVD, control FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1660 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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: Alpha-fetoprotein (AFP) IVD, control
IMMULITE® Systems AFP Calibration Verification Material by Siemens Healthcare Diagnostics Products Ltd — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Alpha-fetoprotein (AFP) IVD, control.
- Alpha-Fetoprotein Control Slides — BIO SB, INC. · Class I
- Alpha-Fetoprotein Control Slides — BIO SB, INC. · Class I
- Atellica IM AFP MCM — Siemens Healthcare Diagnostics · Class I
- Alpha-Fetoprotein control slides — BIO SB, INC. · Class I
- ARCHITECT — Abbott Ireland Diagnostics · Class III
- ADVIA Centaur® Systems, ACS 180® Systems AFP MCM — Siemens Healthcare Diagnostics · Class I
- Alinity — Abbott Ireland Diagnostics · Class III
- AIA-PACK AFP Calibration Verification Test Set — Tosoh Corp. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics Products Ltd
Sources (1)
- FDA UDI 577a748c-fa14-44fe-bbdf-841e79c09e77 37 fields · synced Jun 8, 2026