- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 21, 2026
5060855886SKY830F65 references
5060855886SKY830F6No device characteristics flagged
Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
T01020204Nitrile examination / treatment gloves5 references
| Product | Trade name | Reference / catalog number | Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary → | Quantity | Status |
|---|---|---|---|---|---|
| SKYTEC | SKYTEC | SKG00830DF | 05060855886186 | 100 | On the market |
| SKYTEC | SKYTEC | SKG00830DH | 05060855886193 | 100 | On the market |
| SKYTEC | SKYTEC | SKG00830DL | 05060855886216 | 100 | On the market |
| SKYTEC | SKYTEC | SKG00830DD | 05060855886179 | 100 | On the market |
| SKYTEC | SKYTEC | SKG00830DJ | 05060855886209 | 100 | On the market |