Eu Mdr
Eu Md Class 2a
Not Intended For Eu Market
🇧🇪 Belgium
GAMMEX Latex Dermashield
Devices (same UDI-DI)
8
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 15414566631851
- Basic UDI-DI Code
- 5414566GLDER3300ZN
- Reference
- 330063085 Size 8.5
- Device Types
-
Latex Single use Sterile
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 2a
- Status
- Not Intended For Eu Market
- Manufacturer
- Ansell Healthcare Europe NV
CND Nomenclature Codes
| Code | Description |
|---|---|
| T01010102 | NON-POWDERED LATEX SURGICAL GLOVES |
Related Devices
The Basic UDI-DI associated with this device has 8 devices in total. Below are some other devices sharing the same Basic UDI-DI.
GAMMEX Latex Dermashield
Device
EU MDR
·
Eu Md Class 2a
·Ansell Healthcare Europe NV·Not intended for eu market
GAMMEX Latex Dermashield
Device
EU MDR
·
Eu Md Class 2a
·Ansell Healthcare Europe NV·Not intended for eu market
GAMMEX Latex Dermashield
Device
EU MDR
·
Eu Md Class 2a
·Ansell Healthcare Europe NV·Not intended for eu market
GAMMEX Latex Dermashield
Device
EU MDR
·
Eu Md Class 2a
·Ansell Healthcare Europe NV·Not intended for eu market
GAMMEX Latex Dermashield
Device
EU MDR
·
Eu Md Class 2a
·Ansell Healthcare Europe NV·Not intended for eu market
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