EUDAMED last updated this device on May 27, 2026
AGG/PAK™ 5 Combo Kit
++G05610765056On the marketIVDR Class A
- Applicable legislation
- —
- Organization name
- Bio/Data Corporation
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 →- *+G0561076501/$$1126414000XXX*
- Reference / catalog number
- 107650
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.
AGG/PAK™ 5 Combo Kit is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Bio/Data Corporation. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.