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Doubleflo Inflow/Outflow Pump And Manual
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 72205776Model POMPE D'ARTHROSCOPIERef 72205775FModel POMPE D'ARTHROSCOPIE
by Hemodia Sas
Identity
- Trade Name
- DOUBLEFLO INFLOW/OUTFLOW PUMP AND MANUAL EUDAMEDDOUBLEFLO FDA UDI
- Generic Name
- Arthroscopic irrigation/insufflation system FDA UDI
- Device Name
- POMPE D'ARTHROSCOPIE EUDAMEDDOUBLEFLO INFLOW/OUTFLOW PUMP FDA UDI
- Model / Reference
- POMPE D'ARTHROSCOPIE EUDAMED72205776 EUDAMED72205775F EUDAMEDB1 FDA UDI
- Description
- DOUBLEFLO INFLOW/OUTFLOW PUMP FDA UDI
Identifiers
- Catalog Number
- 72205776 FDA UDI
- Primary DI / UDI-DI
- 03661379211748 EUDAMEDFDA UDI03661379239049 EUDAMED
- Basic UDI-DI
- 3661379FAB010002AE2 EUDAMEDB-03661379239049 EUDAMED
- Direct Marketing DI
- 03661379211748 EUDAMED
- FDA Product Code
- HRX FDA UDI
- EMDN Code
- Z1202110201 MOTORISED ARTHROSCOPIC SURGERY SYSTEMS EUDAMED
- GMDN Term
- Arthroscopic irrigation/insufflation system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMEDEUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Doubleflo Inflow/Outflow Pump And Manual by Hemodia Sas — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 3661379FAB010002AE2 | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 3661379FAB010002AE2 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hemodia Sas
- EUDAMED SRN
- FR-MF-000007191
Sources (3)
- EUDAMED 502db651-c6f4-46b3-8593-fb2120d2b49a 61 fields · synced Jul 9, 2026
- EUDAMED 3f5172df-db3e-4040-823f-80229b7f2803 61 fields · synced May 17, 2026
- FDA UDI 77107bb1-802d-414f-9f99-0f2a92920cc1 34 fields · synced May 30, 2026