Identity
- Trade Name
- PiCCO Monitoring Kit FDA UDI
- Generic Name
- Invasive blood pressure transducer set FDA UDI
- Model / Reference
- PV8103 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04250094500184 FDA UDI
- 510(k) Number
- K991886 FDA UDI
- FDA Product Code
- KRB FDA UDI
- GMDN Term
- Invasive blood pressure transducer set 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
PiCCO Monitoring Kit 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 139b33d2-1ffa-4077-a7fd-7e3d3f4f00d1 35 fields · synced Jun 1, 2026