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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 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Drypro Model 832 | GM76 | FDA UDI | Class II | Active |
| REGIUS Plate | DYEY | FDA UDI | Class II | Active |
| Konicaminolta Di-X1 | ACDX | FDA UDI | Class II | Active |
| Regius Model 110 | JFF7 | FDA UDI | Class II | Active |
| Drypro Model 832 | GNPM | FDA UDI | Class II | Active |
| Drypro Sigma | A4A9 | FDA UDI | Class II | Active |
| Linear Probe L14-4 | A8J9 | FDA UDI | Class II | Active |
| REGIUS Cassette | A2NE | FDA UDI | Class II | Active |
| REGIUS Cassette | A3P1 | FDA UDI | Class II | Active |
| AeroDR P-11 | A5DP | FDA UDI | Class II | Active |
| Drypro Sd-Qm2 | AE6J | FDA UDI | Class I | Active |
| Drypro Sd-P | A5FM | FDA UDI | Class I | Active |
| AeroDR P-52 | A92H | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS1 | AC7H | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS1 | AAEU | FDA UDI | Class II | Active |
| REGIUS Plate | EDNQ | FDA UDI | Class II | Active |
| P-71 | A9YD | FDA UDI | Class II | Active |
| AeroDR T50 | A4UW | FDA UDI | Class II | Active |
| REGIUS Cassette | E2LT | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS1 | AC7J | FDA UDI | Class II | Active |
| ImagePilot | D9MA | FDA UDI | Class II | Active |
| ImagePilot | V1.92R00E | FDA UDI | Class II | Active |
| P-71 | A8CF | FDA UDI | Class II | Active |
| Sr-5c | 1728891A | FDA UDI | Class II | Unknown |
| Ultrasound System SONIMAGE MX1 | AAK9 | FDA UDI | Class II | Active |
| Cs-7 | AEVD | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | KCSK | FDA UDI | Class II | Active |
| AeroDR S33/S30 | AACU | FDA UDI | Class II | Active |
| REGIUS Plate | E264 | FDA UDI | Class II | Active |
| Ultrasound System SONIMAGE HS2 | ADDV | FDA UDI | Class II | Active |
| ImagePilot | V1.94R00E | FDA UDI | Class II | Active |
| REGIUS Cassette | A1PJ | FDA UDI | Class II | Active |
| REGIUS Cassette | A2TC | FDA UDI | Class II | Active |
| Skr 4000 | ACX9 | FDA UDI | Class II | Active |
| AeroDR P-11 | A7WE | FDA UDI | Class II | Active |
| Regius Model 110 | A5RE | FDA UDI | Class II | Active |
| Regius Model Sigma | A1P6 | FDA UDI | Class II | Active |
| ImagePilot | V1.95 | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | KCU5 | FDA UDI | Class II | Active |
| P-65 | A9YJ | FDA UDI | Class II | Active |
| PULSOX-300i | 1732311A | FDA UDI | Class II | Unknown |
| REGIUS Cassette | E2F7 | FDA UDI | Class II | Active |
| Drypro Sd-P | A5FR | FDA UDI | Class I | Active |
| P-81 | A8CG | FDA UDI | Class II | Active |
| REGIUS Cassette/Plate | JFJ8 | FDA UDI | Class II | Active |
| Drypro Sd-Q2 | AE63 | FDA UDI | Class I | Active |
| Drypro Sigma 2 | A9R5 | FDA UDI | Class II | Active |
| REGIUS Cassette | A1PH | FDA UDI | Class II | Active |
| Regius Model Sigma | A1P8 | FDA UDI | Class II | Active |
| Drypro Sd-S | A76F | FDA UDI | Class I | 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. |