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Doubleflo Day Tube Set
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 72205772Model TUBULURE D'ARTHROSCOPIERef 72205772
by Hemodia Sas
Identity
- Trade Name
- DOUBLEFLO DAY TUBE SET EUDAMEDDOUBLEFLO FDA UDI
- Generic Name
- Surgical irrigation/aspiration tubing set FDA UDI
- Device Name
- TUBULURE D'ARTHROSCOPIE EUDAMEDTubulures d'arthroscopie EUDAMEDDOUBLEFLO DAY TUBE SET FDA UDI
- Model / Reference
- TUBULURE D'ARTHROSCOPIE EUDAMED72205772 EUDAMEDA FDA UDI
- Description
- DOUBLEFLO DAY TUBE SET FDA UDI
Identifiers
- Catalog Number
- 72205772 FDA UDI
- Primary DI / UDI-DI
- 03661379223055 EUDAMEDFDA UDI
- Basic UDI-DI
- B-03661379223055 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
No
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 Day 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-03661379223055 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-03661379223055 | 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 2a19e4b4-5a7c-4319-a4cd-aa27ba936110 61 fields · synced Jul 24, 2026
- EUDAMED d73cd8de-57ec-45fb-81b1-85a70d4bbfd1 61 fields · synced May 17, 2026
- FDA UDI 06a1bab2-0d1f-45b9-8aac-b87a54f3e01b 34 fields · synced May 30, 2026