Eu Mdd
Eu Md Class 3
On The Market
๐ฏ๐ต Japan
OSTEOTRANS
Devices (same UDI-DI)
1
Certificates
1
Countries
1
Notified Bodies
1
Basic Information
- Primary DI
- 04550052847970
- Basic UDI-DI Code
- B-04550052847970
- Reference
- OK0730A
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- TEIJIN MEDICAL TECHNOLOGIES CO., LTD.
CND Nomenclature Codes
| Code | Description |
|---|---|
| P09120605 | INTERFERENCE SCREWS |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II (excluding section 4) | 2076971CE01 | DEKRA Certification B.V. | Expired |
Available In Countries
๐ฎ๐น Italy
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