Identity
- Trade Name
- AU FDA UDI
- Generic Name
- LDL (low density lipoprotein) antibody (anti-LDL) IVD, calibrator FDA UDI
- Device Name
- LDL Cholesterol Calibrator FDA UDI
- Model / Reference
- ODC0024 FDA UDI
- Description
- LDL Cholesterol Calibrator FDA UDI
Identifiers
- Primary DI / UDI-DI
- 15099590070519 FDA UDI
- 510(k) Number
- K040471 FDA UDI
- FDA Product Code
- JIT FDA UDI
- GMDN Term
- LDL (low density lipoprotein) antibody (anti-LDL) IVD, calibrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1150 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: LDL (low density lipoprotein) antibody (anti-LDL) IVD, calibrator
Au by Beckman Coulter, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as LDL (low density lipoprotein) antibody (anti-LDL) IVD, calibrator.
- JAS Diagnostics — Drew Scientific , Ltd. · Class I
Cleared under the same submission
K040471 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Beckman Coulter, Inc.
Sources (1)
- FDA UDI e3558437-3e8c-405e-a243-92417e4de5a1 34 fields · synced Jun 8, 2026