FEI 3010850471
Vivonic Gmbh
Kurfuerst-Eppstein-Ring 4, Sailauf Bavaria, DE
MDR events334All time
Recalls0All time
Registered products1
Establishment typeManufactureManufacture Medical Device
Registered product codes
1 product codes
Recent MDR events
334 on file
- AQUABPLUS 2500 B2 2000Jun 16, 2026Malfunction3010850471-2026-00007
- AQUABPLUS 2500 B2 2000Apr 16, 2026Malfunction3010850471-2026-00006
- AQUABPLUS 2500 B2 2000Mar 18, 2026Malfunction3010850471-2026-00005
- AQUABPLUS 2500 B2 2000Feb 17, 2026Malfunction3010850471-2026-00004
- AQUABPLUS 2000 B2 1500Feb 5, 2026Malfunction3010850471-2026-00003
- AQUAA 1800 A2 1800HJan 14, 2026Malfunction3010850471-2026-00002
- AQUABPLUS 2000 B2 1500Jan 12, 2026Malfunction3010850471-2026-00001
- AQUAA 2700HOct 29, 2025Malfunction3010850471-2025-00016
- AQUABPLUS 2500 B2 2000Oct 21, 2025Malfunction3010850471-2025-00015
- AQUABPLUS 1500 B2 1000Aug 18, 2025Malfunction3010850471-2025-00014
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 3010850471.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.