FEI 3006554912
Steris Deutschland Gmbh
KANTSTRASSE 33/1, Wurmlingen Baden-Wurttemberg, DE
MDR events9All time
Recalls0All time
Registered products162
Establishment typeRepackRepack or Relabel Medical Device
Registered product codes
162 product codes
Recent MDR events
9 on file
- V. MuellerJul 10, 2026Malfunction3006554912-2026-00007
- V. MUELLERMay 28, 2026Malfunction3006554912-2026-00006
- V. MUELLERApr 24, 2026Malfunction3006554912-2026-00005
- V. MUELLERApr 3, 2026Malfunction3006554912-2026-00004
- V. MUELLERMar 25, 2026Malfunction3006554912-2026-00003
- SNOWDEN-PENCERJan 28, 2026Malfunction3006554912-2026-00002
- V. MUELLERJan 16, 2026Malfunction3006554912-2026-00001
- V. MUELLERNov 19, 2025Malfunction3006554912-2025-00002
- V. MUELLERNov 13, 2025Malfunction3006554912-2025-00001
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 3006554912.
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.