Identity
- Trade Name
- RAPIDPoint® 400 Measurement Cartridge FDA UDI
- Generic Name
- Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent FDA UDI
- Device Name
- RAPIDPoint® 400 Measurement Cartridge (400 tests) - pH, pCO2, pO2, Na+, Ca++, Cl-, K+, Glu, Hct. For in vitro diagnostic use with RAPIDPoint ® 400 systems. FDA UDI
- Model / Reference
- 10329756 FDA UDI
- Description
- RAPIDPoint® 400 Measurement Cartridge (400 tests) - pH, pCO2, pO2, Na+, Ca++, Cl-, K+, Glu, Hct. For in vitro diagnostic use with RAPIDPoint ® 400 systems. FDA UDI
Identifiers
- Catalog Number
- 130517 FDA UDI
- Primary DI / UDI-DI
- 00630414469225 FDA UDI
- 510(k) Number
- K002738 FDA UDI
- FDA Product Code
- GKF FDA UDICEM FDA UDICGZ FDA UDICGA FDA UDIJGS FDA UDIJFP FDA UDICHL FDA UDI
- GMDN Term
- Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.5600 FDA UDI862.1600 FDA UDI862.1170 FDA UDI862.1345 FDA UDI862.1665 FDA UDI862.1145 FDA UDI862.1120 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent
RAPIDPoint® 400 Measurement Cartridge by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent.
- i-STAT — Abbott Point of Care Inc. · Class II
- Synermed® — INFRARED LABORATORY SYSTEMS LLC · Class II
- i-STAT — Abbott Point of Care Inc. · Class II
- PHOENIX DIAGNOSTICS, INC. — PHOENIX DIAGNOSTICS, INC. · Class II
- H4 Cartridge — Lifehealth · Class II
- i-STAT — Abbott Point of Care Inc. · Class I
- Phoenix Diagnostics — PHOENIX DIAGNOSTICS, INC. · Class II
- Synermed® — INFRARED LABORATORY SYSTEMS LLC · Class II
Cleared under the same submission
K002738 also covers:
- RAPIDPoint® 400 Measurement Cartridge — Siemens Healthcare Diagnostics
- RAPIDPoint® 400/405/500 Wash/Waste Cartridge — Siemens Healthcare Diagnostics
- RAPIDPoint® 400/405/500 Wash/Waste Cartridge — Siemens Healthcare Diagnostics
- RAPIDPoint® 400/405/500 Wash/Waste Cartridge — Siemens Healthcare Diagnostics
- RAPIDSystems™ AutomaticQC Cartridge — Siemens Healthcare Diagnostics
- RAPIDSystems™ AutomaticQC Cartridge — Siemens Healthcare Diagnostics
- TB1 pO2/pCO2 Test/Blank Sensor — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI 6f9fe7a7-657e-4843-9d43-3fc34d8efd46 37 fields · synced May 31, 2026