Identity
- Trade Name
- Alere Cholestech LDX® FDA UDI
- Generic Name
- Multiple lipid analyte IVD, reagent FDA UDI
- Device Name
- Alere Cholestech LDX® TC GLU FDA UDI
- Model / Reference
- 10-988 FDA UDI
- Description
- Alere Cholestech LDX® TC GLU FDA UDI
Identifiers
- Catalog Number
- 10-988 FDA UDI
- Primary DI / UDI-DI
- 00893038002623 FDA UDI
- FDA Product Code
- CHH FDA UDICGA FDA UDI
- GMDN Term
- Multiple lipid analyte IVD, reagent FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1175 FDA UDI862.1345 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Alere Cholestech LDX® by Alere San Diego, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Alere San Diego, Inc.
Sources (1)
- FDA UDI 0f85d5a6-faf4-499b-933e-f9eb51294250 37 fields · synced Jun 9, 2026