Plastipak
by Becton, Dickinson and Company 2 variants
Ref 305502
Active
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/MDD | NumberB-0038290550201LEY D-0038290550201LEY | Date23 Oct 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device name
- BD PlastipakTM 1mL Sub-Q 0,40mm (27G) x 10mm
- Model / reference
- 305502
- Primary DI / UDI-DI
- D-0038290550201LEY
- Basic UDI-DI
- B-0038290550201LEY
- EMDN code
- A0101010102 Hypodermic syringe needles, w/o safety systems
- Device class
- Class IIa
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- US-MF-000019182
- Authorised representative
- Becton Dickinson France SAS FR-AR-000011519
Other devices from Becton, Dickinson and Company
Properties
Other properties (13)
- Sterilise before use: No
- Implantable: No
- Reusable: 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