Identity
- Trade Name
- Dimension® Flex® reagent cartridge CRE2 FDA UDI
- Generic Name
- Creatinine IVD, kit, spectrophotometry FDA UDI
- Device Name
- Creatinine Flex® reagent cartridge, 480 tests FDA UDI
- Model / Reference
- 10872079 FDA UDI
- Description
- Creatinine Flex® reagent cartridge, 480 tests FDA UDI
Identifiers
- Catalog Number
- DF33B FDA UDI
- Primary DI / UDI-DI
- 00630414595009 FDA UDI
- 510(k) Number
- K132638 FDA UDI
- FDA Product Code
- CGX FDA UDI
- GMDN Term
- Creatinine IVD, kit, spectrophotometry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1225 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
No
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: Creatinine IVD, kit, spectrophotometry
Dimension® Flex® reagent cartridge CRE2 by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Creatinine IVD, kit, spectrophotometry.
- CREATININE-S Assay — Sekisui Diagnostics, LLC · Class II
- Creatinine Jaff method — Roche Diagnostics Corp. · Class II
- Yumizen C1200 Creatinine Jaffé — Horiba Abx · Class II
- Carolina Liquid Chemistries Corp. Basic Multi-Drug Control Set — Carolina Liquid Chemistries Corp. · Class I
- Diazyme — Diazyme Laboratories, Inc.
- CREATININE (CREA) — Randox Laboratories, Ltd. · Class II
- Creatinine Jaff Gen2 — Roche Diagnostics Corp. · Class II
- ARCHITECT — Abbott Laboratories, Inc. · Class II
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
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI a821bdda-760c-4118-a706-ad9af4a02b7a 37 fields · synced May 30, 2026