Identity
- Trade Name
- Futhrough EUDAMED
- Device Name
- Futhrough™ Endovascular needle system EUDAMED
- Model / Reference
- LT-FIS-20G5F080 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06938370136095 EUDAMED
- Basic UDI-DI
- B-06938370136095 EUDAMED
- EMDN Code
- A01010302 NEEDLES AND KITS FOR IMPLANTABLE SYSTEMS (PORT), W/O SAFETY SYSTEMS EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Greece EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Futhrough by Lifetech Scientific (Shenzhen) Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06938370136095 | Class III | Active |
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Manufacturer
- Manufacturer
- Lifetech Scientific (Shenzhen) Co., Ltd.
- EUDAMED SRN
- CN-MF-000001561
- Authorised Representative
- LifeTech Scientific (Europe) B.V. NL-AR-000000804
Sources (1)
- EUDAMED a1f1332a-35fc-4840-934b-e3da9b1fd833 61 fields · synced Jun 19, 2026