Devices (same UDI-DI)
1
Certificates
1
Countries
20
Notified Bodies
1
Basic Information
- Primary DI
- 07290016441093
- Basic UDI-DI Code
- B-07290016441093
- Reference
- FG0009
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- Perflow Medical Ltd.
Additional Description
Non-Occlusive Remodeling Net
CND Nomenclature Codes
| Code | Description |
|---|---|
| C99 | CARDIOCIRCULATORY DEVICES - OTHER |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II Section 4 | 170769617 | DQS Medizinprodukte GmbH | Expired |
Available In Countries
๐ฆ๐น Austria
๐ง๐ช Belgium
๐จ๐พ Cyprus
๐ฉ๐ช Germany
๐ฉ๐ฐ Denmark
๐ช๐ช Estonia
๐ฌ๐ท Greece
๐ช๐ธ Spain
๐ซ๐ฎ Finland
๐ซ๐ท France
๐ฎ๐น Italy
๐ฑ๐น Lithuania
๐ฑ๐ป Latvia
๐ณ๐ฑ Netherlands
๐ณ๐ด Norway
๐ต๐ฑ Poland
๐ต๐น Portugal
๐ธ๐ช Sweden
๐น๐ท Tรผrkiye
๐ฌ๐ง United Kingdom
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDD).
SafeSept Transseptal Guidewire
Device
EU MDD
·
Eu Md Class 3
·Pressure Products Medical Device Manufacturing LLC.·On the market·32 countries
PTCA BALLOON DILATION CATHETERS
Device
EU MDD
·
Eu Md Class 3
·BrosMed Medical Co., Ltd·On the market·32 countries
PTCA BALLOON DILATION CATHETERS
Device
EU MDD
·
Eu Md Class 3
·BrosMed Medical Co., Ltd·On the market·32 countries
Cutanplast Standard
Device
EU MDD
·
Eu Md Class 3
·Mascia Brunelli S.p.A.·On the market·21 countries
PTCA BALLOON DILATION CATHETERS
Device
EU MDD
·
Eu Md Class 3
·BrosMed Medical Co., Ltd·On the market·32 countries
PTCA BALLOON DILATION CATHETERS
Device
EU MDD
·
Eu Md Class 3
·BrosMed Medical Co., Ltd·On the market·32 countries