Eu Mdr
Eu Md Class 1
No Longer On The Market
Laminoitu leikkaustakki S
Vahvistettu leikkaustakki
Devices (same UDI-DI)
5
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 06430076980113
- Basic UDI-DI Code
- 643007698002AZ
- Reference
- 38971129
- Device Types
-
Sterile Sterilization
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 1
- Status
- No Longer On The Market
Additional Description
Toimenpidepakkaus sisältää CE merkityn vahvistetun leikkaustakin Laminoitu leikkaustakki S
Medical Purpose
Vahvistettu leikkaustakki
CND Nomenclature Codes
| Code | Description |
|---|---|
| T020402 | REINFORCED SURGICAL GOWNS |
Related Devices
The Basic UDI-DI associated with this device has 5 devices in total. Below are some other devices sharing the same Basic UDI-DI.
Laminoitu leikkaustakki XXL
Device
EU MDR
·
Eu Md Class 1
·No longer on the market
Laminoitu leikkaustakki XL
Device
EU MDR
·
Eu Md Class 1
·No longer on the market
Laminoitu leikkaustakki L
Device
EU MDR
·
Eu Md Class 1
·No longer on the market
Laminoitu leikkaustakki M
Device
EU MDR
·
Eu Md Class 1
·No longer on the market
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