Identity
- Trade Name
- L-Type LDL-C Reagent 2 FDA UDI
- Generic Name
- Low density lipoprotein (LDL) cholesterol IVD, reagent FDA UDI
- Device Name
- In-Vitro Diagnostic Use FDA UDI
- Model / Reference
- 999-00504 FDA UDI
- Description
- In-Vitro Diagnostic Use FDA UDI
Identifiers
- Catalog Number
- 999-00504 FDA UDI
- Primary DI / UDI-DI
- 14987481164540 FDA UDI
- 510(k) Number
- K982271 FDA UDI
- FDA Product Code
- LBR FDA UDI
- GMDN Term
- Low density lipoprotein (LDL) cholesterol IVD, reagent FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1475 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
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: Low density lipoprotein (LDL) cholesterol IVD, reagent
L-Type LDL-C Reagent 2 by Fujifilm Wako Pure Chemical Corporation — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Low density lipoprotein (LDL) cholesterol IVD, reagent.
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Cleared under the same submission
K982271 also covers:
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | IVDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Fujifilm Wako Pure Chemical Corporation
Sources (2)
- FDA UDI ef24b186-5326-42e3-9c9e-318f4637d6a4 37 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 5, 2026