Identity
- Trade Name
- Dimension® CHOL Calibrator FDA UDI
- Generic Name
- Total cholesterol lipid IVD, calibrator FDA UDI
- Device Name
- Cholesterol Calibrator, 2x3x1mL FDA UDI
- Model / Reference
- 10444998 FDA UDI
- Description
- Cholesterol Calibrator, 2x3x1mL FDA UDI
Identifiers
- Catalog Number
- DC16 FDA UDI
- Primary DI / UDI-DI
- 00842768004957 FDA UDI
- 510(k) Number
- K861700 FDA UDI
- FDA Product Code
- JIX FDA UDI
- GMDN Term
- Total cholesterol lipid 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
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
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: Total cholesterol lipid IVD, calibrator
Dimension® CHOL Calibrator by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Total cholesterol lipid IVD, calibrator.
- FORA — FORA CARE INC. · Class I
- Pointe Scientific, Inc. — POINTE SCIENTIFIC, INC. · Class I
- POINTE SCIENTIFIC Cholesterol Standard — POINTE SCIENTIFIC, INC. · Class I
- Direct (HDL/LDL) Cholesterol Calibrator — STANBIO LABORATORY, L.P. · Class I
- Matrix Plus Cholesterol, Level F — VERICHEM LABORATORIES, INC. · Class II
- HDL Cholesterol Verifier Kit — VERICHEM LABORATORIES, INC. · Class II
- Cholesterol Reference Kit — VERICHEM LABORATORIES, INC. · Class II
Cleared under the same submission
K861700 also covers:
- Dimension® CHEM II Calibrator — Siemens Healthcare Diagnostics
- Dimension® Flex® reagent cartridge ALB — Siemens Healthcare Diagnostics
- Dimension® Flex® reagent cartridge CHOL — Siemens Healthcare Diagnostics
- Dimension® Flex® reagent cartridge GGT — Siemens Healthcare Diagnostics
- Dimension® Flex® reagent cartridge MG — Siemens Healthcare Diagnostics
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 |
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Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI 79c84793-52f8-45b2-ab36-4755850c545d 37 fields · synced Jun 1, 2026