Surpass
Let the assistant research this device
The Research Assistant compiles risk class, certificates, notified bodies and related records โ and cites every one.
Free to try ยท every answer cites its records
Basic Information
- Primary DI
- 06938370135074
- Basic UDI-DI Code
- B-06938370135074
- Reference
- SSGW-35-260
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 2a
- Status
- On The Market
- Manufacturer
- Lifetech Scientific (Shenzhen) Co., Ltd.
Additional Description
The SurpassTM Super Stiff Guidewire is a PTFE-coated stainless steel Guidewire. It has 4 cm of tip flexibility including an inner gold coil for enhanced visibility. The Guidewire is used both to assist anatomical access for other devices (not included), and to support the delivery of medical devices. The Guidewire is introduced into the target vessel; other devices, such as a sheath, catheter, stent, or endovascular graft can then be passed over the Guidewire to be positioned or manipulated within the vascular system.
CND Nomenclature Codes
| Code | Description |
|---|---|
| C04020202 | PERIPHERAL VASCULAR THERAPEUTIC GUIDEWIRES, NON-HYDROPHILIC |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II (excluding section 4) | 2107231CE01 | DEKRA Certification B.V. | Expired |
Available In Countries
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 2a) and regulation (EU MDD).