EUDAMED last updated this device on Jul 8, 2026
InSync LINER / TITAN-OPAQUE LIQUID
42520058001H8- Applicable legislation
- —
- Organization name
- Chemichl AG
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 →- 04252005830021
- Reference / catalog number
- 0801
InSync LINER / TITAN-OPAQUE LIQUID is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Chemichl AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.