Devices (same UDI-DI)
1
Certificates
1
Countries
11
Notified Bodies
1
Basic Information
- Primary DI
- 05206913006442
- Basic UDI-DI Code
- B-05206913006442
- Reference
- PR200D
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- TH.KAZANTZIDIS SA - MEDIPAC
CND Nomenclature Codes
| Code | Description |
|---|---|
| H010201010501 | POLYTETRAFLUOROETHYLENE (PTFE) MONOFILAMENT WITH NEEDLE |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II (excluding section 4) | 301041049 | NATIONAL EVALUATION CENTER OF QUALITY AND TECHNOLOGY IN HEALTH S.A.- EKAPTY | Expired |
Available In Countries
🇦🇹 Austria
🇧🇬 Bulgaria
🇨🇾 Cyprus
🇩🇪 Germany
🇬🇷 Greece
🇪🇸 Spain
🇫🇷 France
🇮🇹 Italy
🇵🇹 Portugal
🇷🇴 Romania
🇸🇪 Sweden
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