Current™
by Abbott Medical EUDAMEDGUDID
Active
Ref PFA-GEN-V102
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number5414734ABC00456P | Date24 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05415067053893 | Date20 Apr 2026 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Generic Name
- Cardiac irreversible electroporation system generator
- Device Name
- PFA Generator
- Model / Ref / Catalog
- PFA-GEN-V102
- Primary DI / UDI-DI
- 05415067053893
- Basic UDI-DI
- 5414734ABC00456P
- PMA Number
- FDA Product Code
- QZI
- EMDN Code
- Z12059011 Cardiac ablation equipment
- GMDN Term
- Cardiac irreversible electroporation system generator
- Device Class
- Class IIb EUDAMEDClass III GUDID
- Market of Registration
- Belgium
- Commercial Distribution
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIb | Class III |
Manufacturer details
- EUDAMED SRN
- US-MF-000033655
- Authorised representative
- Abbott Medical BE-AR-000008744
Other devices from Abbott Medical
Properties
Other properties (20)
- Sterile: No
- Single Use: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No