Futhrough
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Basic Information
- Primary DI
- 06938370136125
- Basic UDI-DI Code
- B-06938370136125
- Reference
- LT-FIS-17G9F045B
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- Lifetech Scientific (Shenzhen) Co., Ltd.
Additional Description
FuthroughTM Endovascular Needle System is used as an auxiliary device, through percutaneous puncture, with the information of location, direction and X-ray visible status for In-situ fenestration after thoracic aorta stent implantation. FuthroughTM Endovascular Needle System consists of two types, with and without balloon. The system with balloon consists of an anchoring balloon and a puncturing needle, and the anchoring balloon and the puncturing needle are assembled together.
CND Nomenclature Codes
| Code | Description |
|---|---|
| A01010302 | NEEDLES AND KITS FOR IMPLANTABLE SYSTEMS (PORT), W/O SAFETY SYSTEMS |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II Section 4 | 2107231DE07 | DEKRA Certification B.V. | Expired |
Available In Countries
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDD).