Is this your brand? Sign in to claim ownership.
Sign in to claim this brandKonica Minolta, Inc.
Japan·JP-MF-000008214
Last updated September 17, 2026
Information
- Country
- Japan
- Address
- 1, Sakura-machi, Tokyo, Japan
- Website
- konicaminolta.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Sato Yoshinori
- EUDAMED SRN
- JP-MF-000008214
- FDA FEI Number
- 3004485675
- DUNS Number
- 692076161
Catalogue (192)
Page 2 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| REGIUS Cassette | A2VX | FDA UDI | Class II | Active |
| Konicaminolta Di-X1 | AEYC | FDA UDI | Class II | Active |
| G-22 | AE83 | FDA UDI | Class II | Active |
| AeroDR P-21 | A6C3 | FDA UDI | Class II | Active |
| Linear Probe L11-3 | A9E5 | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | KCPJ | FDA UDI | Class II | Active |
| REGIUS Plate | EDE3 | FDA UDI | Class II | Active |
| Regius Model Sigma2 | A5ET | FDA UDI | Class II | Active |
| REGIUS Cassette | A2RS | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | KCKD | FDA UDI | Class II | Active |
| P-75 | A9YT | FDA UDI | Class II | Active |
| P-75 | ADA6 | FDA UDI | Class II | Unknown |
| REGIUS Plate | ED7W | FDA UDI | Class II | Active |
| Regius Model 210 | A1YD | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS1 | A8AR | FDA UDI | Class II | Active |
| P-82 | ADU6 | FDA UDI | Class II | Active |
| Drypro Sd-P | A5FH | FDA UDI | Class I | Active |
| Bone Suppression Software | AEVM | FDA UDI | Class II | Active |
| AeroDR P-52 | A6C7 | FDA UDI | Class II | Active |
| P-95 | ADU3 | FDA UDI | Class II | Active |
| REGIUS Plate | ED64 | FDA UDI | Class II | Active |
| G-59 | AE81 | FDA UDI | Class II | Active |
| Drypro Sd-Qm2 | AE6H | FDA UDI | Class I | Active |
| P-41 | ACNN | FDA UDI | Class II | Active |
| Konicaminolta Di-X1 | AE9A | FDA UDI | Class II | Active |
| REGIUS Plate | P49C | FDA UDI | Class II | Active |
| Regius Model 110 | A5RD | FDA UDI | Class II | Active |
| Drypro Sd-Q2 | AE62 | FDA UDI | Class I | Active |
| Drypro Sd-P | A5FJ | FDA UDI | Class I | Active |
| AeroDR P-31 | A7XT | FDA UDI | Class II | Active |
| AeroDR X70 | AACT | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS1 | A7AP | FDA UDI | Class II | Active |
| AeroDR P-51 | A7VY | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | KC6G | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | BUN2 | FDA UDI | Class II | Active |
| Endocavity Probe EC9-3 | A96C | FDA UDI | Class II | Active |
| P-95 | ADU1 | FDA UDI | Class II | Active |
| P-81 | A9YE | FDA UDI | Class II | Active |
| P-61 | A8CE | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS1 | A9RP | FDA UDI | Class II | Active |
| AeroDR P-51 | A8HP | FDA UDI | Class II | Active |
| G-60 | AE82 | FDA UDI | Class II | Active |
| Linear Probe HL18-4 | A9E3 | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | KCMM | FDA UDI | Class II | Active |
| P-53 | AEA1 | FDA UDI | Class II | Active |
| Drypro Sd-Qm | A3RJ | FDA UDI | Class I | Active |
| AeroDR 0170CS | AACW | FDA UDI | Class II | Active |
| Regius Model Sigma2 | A5ER | FDA UDI | Class II | Active |
| REGIUS Plate | EDDM | FDA UDI | Class II | Active |
| REGIUS Cassette | A3P4 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 24, 2017 | Z-2769-2017 | — | terminated | The Doppler velocity measurement on the Sonimage HS1 ultrasound system is not accurate. |