Acu-Punch
Ref P510
Acu-Punch (P510) is a Class IIa device made by Acuderm, Inc., registered in EUDAMED on 11 May 2026 (Basic UDI-DI B-00814105021507), active as of 25 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-00814105021507 00814105021507 | Date11 May 2026 | StatusActive |
Official records
- EUDAMED public site B-00814105021507
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Model / reference
- P510
- Primary DI / UDI-DI
- 00814105021507
- Basic UDI-DI
- B-00814105021507
- EMDN code
- A01020302 Cutaneous biopsy punches, single-use
- Device class
- Class IIa
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- US-MF-000033406
- Authorised representative
- Emergo Europe B.V. NL-AR-000000116
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