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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 1 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Aec6 | AEC6 | EUDAMED | Class I | Active |
| Convex Probe C5-2 | A7C9 | FDA UDI | Class II | Active |
| P-75 | A9YH | FDA UDI | Class II | Active |
| Convex Probe MC10-3 | A9E0 | FDA UDI | Class II | Active |
| P-85 | ADU0 | FDA UDI | Class II | Active |
| Cs-7 | AEVE | FDA UDI | Class II | Active |
| AeroDR P-21 | A7XP | FDA UDI | Class II | Active |
| Drypro Sd-Pm | A5G5 | FDA UDI | Class I | Active |
| Drypro Sd-Q | A3R5 | FDA UDI | Class I | Active |
| Ultrasound System SONIMAGE HS1 | AC7G | FDA UDI | Class II | Active |
| Drypro Sigma 2 | A9R4 | FDA UDI | Class II | Active |
| Drypro Sd-Pm | A5G4 | FDA UDI | Class I | Active |
| Drypro Sd-Qm | A3RK | FDA UDI | Class I | Active |
| Drypro Sd-Q2 | AE65 | FDA UDI | Class I | Active |
| Sector Probe S4-2 | A7CA | FDA UDI | Class II | Active |
| Drypro Model 873 | AE1T | FDA UDI | Class II | Active |
| REGIUS Plate | EDQY | FDA UDI | Class II | Active |
| P-65 | A9YF | FDA UDI | Class II | Active |
| Pulsox-300 | 1732301A | FDA UDI | Class II | Unknown |
| Drypro Model 873 | A2MM | FDA UDI | Class II | Active |
| Linear Probe L18-4 | A7C8 | FDA UDI | Class II | Active |
| P-61 | A9YC | FDA UDI | Class II | Active |
| Konicaminolta Di-X1 | ACDY | FDA UDI | Class II | Active |
| Drypro Sd-S | A76G | FDA UDI | Class I | Active |
| Drypro Sd-Q | A3R6 | FDA UDI | Class I | Active |
| REGIUS Cassette/Plate | KCQ0 | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS1 | A8WA | FDA UDI | Class II | Active |
| P-82 | ADU4 | FDA UDI | Class II | Active |
| Lm-5c | 1728800 | FDA UDI | Class II | Unknown |
| REGIUS Cassette/Plate | KCLU | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | KCWQ | FDA UDI | Class II | Active |
| AeroDR P-31 | A5TE | FDA UDI | Class II | Active |
| REGIUS Cassette | A1PG | FDA UDI | Class II | Active |
| AeroDR P-12 | A85U | FDA UDI | Class II | Active |
| Drypro Sd-Q2 | AE5X | FDA UDI | Class I | Active |
| P-81 | ADA7 | FDA UDI | Class II | Active |
| REGIUS Plate | EDFV | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | KCTC | FDA UDI | Class II | Active |
| P-65 | ADA5 | FDA UDI | Class II | Unknown |
| Drypro Sd-Qm2 | AE6G | FDA UDI | Class I | Active |
| Drypro Sd-Q2 | AE5Y | FDA UDI | Class I | Active |
| Regius Model Sigma2 | A5EU | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS2 | ADDW | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE MX1 | ADRH | FDA UDI | Class II | Active |
| REGIUS Cassette | A3P6 | FDA UDI | Class II | Active |
| REGIUS Cassette | A1GU | FDA UDI | Class II | Active |
| AeroDR P-12 | A50D | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS1 | A9RR | FDA UDI | Class II | Active |
| Drypro Model 873 | A2GP | FDA UDI | Class II | Active |
| REGIUS Cassette | E2E3 | FDA UDI | Class II | Active |
Related Companies
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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. |