Identity
- Trade Name
- PiCCO Catheter FDA UDI
- Generic Name
- Thermal dilution peripheral artery catheter FDA UDI
- Device Name
- 4F Thermodilution catheter, 22cm FDA UDI
- Model / Reference
- PV2014L22N FDA UDI
- Description
- 4F Thermodilution catheter, 22cm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04250094500665 FDA UDI
- 510(k) Number
- K072364 FDA UDI
- FDA Product Code
- KRB FDA UDI
- GMDN Term
- Thermal dilution peripheral artery catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1915 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Dimensions & Sizes
- Size
- Catheter Gauge — 4 French FDA UDILength — 22 Centimeter FDA UDI
PiCCO Catheter by Pulsion Medical Systems SE — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Pulsion Medical Systems SE
Sources (1)
- FDA UDI 2f686605-42dd-48e7-a092-ee91f35d4555 37 fields · synced May 30, 2026