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Doubleflo Patient Tube Set
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 72205773Model TUBULURE D'ARTHROSCOPIE
by Hemodia Sas
Identity
- Trade Name
- DOUBLEFLO PATIENT TUBE SET EUDAMEDDOUBLEFLO FDA UDI
- Generic Name
- Surgical irrigation/aspiration tubing set FDA UDI
- Device Name
- TUBULURE D'ARTHROSCOPIE EUDAMEDTubulures d'arthroscopie EUDAMEDDOUBLEFLO PATIENT TUBE SET FDA UDI
- Model / Reference
- TUBULURE D'ARTHROSCOPIE EUDAMED72205773 EUDAMEDA FDA UDI
- Description
- DOUBLEFLO PATIENT TUBE SET FDA UDI
Identifiers
- Catalog Number
- 72205773 FDA UDI
- Primary DI / UDI-DI
- 03661379223062 EUDAMEDFDA UDI
- Basic UDI-DI
- B-03661379223062 EUDAMED3661379FAB020002AEF EUDAMED
- FDA Product Code
- HRX FDA UDI
- EMDN Code
- A0399 TUBULAR DEVICES - OTHER EUDAMED
- GMDN Term
- Surgical irrigation/aspiration tubing set 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
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Doubleflo Patient Tube Set by Hemodia Sas — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-03661379223062 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-03661379223062 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Hemodia Sas
- EUDAMED SRN
- FR-MF-000007191
Sources (3)
- EUDAMED 94808e34-8f2e-4bbe-8803-9269f54e0884 61 fields · synced Jul 9, 2026
- EUDAMED 9a2e5b27-32f2-483d-a835-681d688dee7d 61 fields · synced May 19, 2026
- FDA UDI 14b88223-8586-4589-9438-dbd11240bd33 34 fields · synced May 30, 2026