EUDAMED last updated this device on Jul 21, 2026
90059GMH
B-IEMF0000137040000013POn the marketClass IIb
- Applicable legislation
- —
- Organization name
- AMO Ireland
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 →- D-IEMF0000137040000013P
- Reference / catalog number
- 90059GMH
Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.
90059GMH is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by AMO Ireland. Placed on the EU market in Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.