EUDAMED last updated this device on Mar 30, 2026
JMS A.V. Fistula Needle Set
B-58888483003476- Applicable legislation
- —
- Organization name
- JMS Singapore Pte Ltd
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 →- 58888483003476
- Reference / catalog number
- 823-1633
JMS A.V. Fistula Needle Set is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by JMS Singapore Pte Ltd. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.