Albania AKBPM registration 11268RD Standart False Bottom Tube
- Risk Class
- Invitro
- Product Model
- RD Standart False Bottom Tube: 04740955001 (UDI-DI 761333601954BG)
- Product Name
- RD Standart False Bottom Tube
- Registration Date
- February 18, 2022
- Analysis ID
- 11268
Tuba sekondare serumi per perdorim ne pajisjet e laboratorit
Access comprehensive regulatory information for RD Standart False Bottom Tube in the Albania medical device market through Pure Global AI's free database. This Invitro medical device is manufactured by Roche Diagnostics GmbH, Sandhofer Strasse 116, 68305 Mannheim, Germany. The device was registered on February 18, 2022.
This page provides complete registration details including product model (RD Standart False Bottom Tube: 04740955001 (UDI-DI 761333601954BG)), manufacturer information, risk classification, and regulatory compliance data from the official Albania medical device database. Pure Global AI offers free access to Albania's medical device registry, helping global MedTech companies navigate Albania regulations efficiently.