Identity
- Trade Name
- CardioChek FDA UDI
- Generic Name
- Multiple lipid analyte IVD, kit, spectrophotometry FDA UDI
- Device Name
- CardioChek Lipid Panel Test FDA UDI
- Model / Reference
- 5700414 FDA UDI
- Description
- CardioChek Lipid Panel Test FDA UDI
Identifiers
- Catalog Number
- 5700414 FDA UDI
- Primary DI / UDI-DI
- 10304040037741 FDA UDI
- FDA Product Code
- LBR FDA UDICHH FDA UDIJGY FDA UDI
- GMDN Term
- Multiple lipid analyte IVD, kit, spectrophotometry FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1475 FDA UDI862.1175 FDA UDI862.1705 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
Yes
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: Multiple lipid analyte IVD, kit, spectrophotometry
CardioChek by Henry Schein, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Multiple lipid analyte IVD, kit, spectrophotometry.
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Cleared under the same submission
K022898 also covers:
- CardioChek — HENRY SCHEIN, INC.
- CardioChek Plus Home Lipid + eGLU Smart Bundle Self-Test 2ct — Polymer Technology Systems
- CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk) — Polymer Technology Systems
- CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk) — Polymer Technology Systems
K023558 also covers:
- CardioChek — HENRY SCHEIN, INC.
- CardioChek Plus Home Lipid + eGLU Smart Bundle Self-Test 2ct — Polymer Technology Systems
- CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk) — Polymer Technology Systems
- CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk) — Polymer Technology Systems
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
- Henry Schein, Inc.
Sources (1)
- FDA UDI fb04be17-469f-4e0d-a436-1b97e3b72731 36 fields · synced May 30, 2026