EUDAMED last updated this device on Sep 9, 2026
sukki
B-06926973979683- Applicable legislation
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- Organization name
- Shandong Haidike Medical Products Co 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 →- 06926973979683
- Reference / catalog number
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sukki is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Shandong Haidike Medical Products Co Ltd. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.