Pressensa Vitalissa Strong Booster
by I.R.A. Istituto Ricerche Applicate S.p.A. EUDAMED
Active
Ref 40404
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-PressensaVitalissa-SBCX | Date21 Aug 2026 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
European Union — CE/MDD Expiring
EU market availability
Made available in 27 countries, as listed in EUDAMED:
- Austria since 17 Oct 2025
- Belgium since 17 Oct 2025
- Bulgaria since 17 Oct 2025
- Croatia since 17 Oct 2025
- Cyprus since 17 Oct 2025
- Czechia since 17 Oct 2025
- Denmark since 17 Oct 2025
- Estonia since 17 Oct 2025
- Finland since 17 Oct 2025
- France since 17 Oct 2025
- Germany since 17 Oct 2025
- Greece since 17 Oct 2025
- Hungary since 17 Oct 2025
- Ireland since 17 Oct 2025
- Italy since 17 Oct 2025
- Latvia since 17 Oct 2025
- Lithuania since 17 Oct 2025
- Luxembourg since 17 Oct 2025
- Malta since 17 Oct 2025
- Netherlands since 17 Oct 2025
- Poland since 17 Oct 2025
- Portugal since 17 Oct 2025
- Romania since 17 Oct 2025
- Slovakia since 17 Oct 2025
- Slovenia since 17 Oct 2025
- Spain since 17 Oct 2025
- Sweden since 17 Oct 2025
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Specification
- Device Name
- Pressensa Vitalissa Strong Booster
- Model / Reference
- 40404
- Primary DI / UDI-DI
- D-PressensaVitalissa-SBCX
- Basic UDI-DI
- B-PressensaVitalissa-SBCX
- EMDN Code
- P900402 Resorbable filling and reconstruction devices
- Device Class
- Class III
- Market of Registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000009981
Other devices from I.R.A. Istituto Ricerche Applicate S.p.A.
See all devices from I.R.A. Istituto Ricerche Applicate S.p.A. →
Properties
Other properties (9)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No