Box
Ref H0040200089Model Box
Active
CE MDR CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberB-08055727377043 08055727377043 | Date10 Jun 2026 | StatusActive |
| European Union | CE/MDD | NumberB-08055727377043 08055727377043 | Date10 Jun 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Model / reference
- Box, H0040200089
- Primary DI / UDI-DI
- 08055727377043
- Basic UDI-DI
- B-08055727377043, 805796871TF0160001V4
- Direct marketing DI
- 08055727377043
- EMDN code
- V0499 Clinical use containers (non-IVD) - other
- Device class
- Class I
- EU registration type
- Legacy device (under a directive)Standard device
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000017541
Other devices from Hpf S.R.L.
Properties
Other properties (12)
- Supplied sterile: No
- Implantable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No