Pure Global

KONICA MINOLTA AeroDR 3 Series - HSA Registration DE0510609

Access comprehensive regulatory information for KONICA MINOLTA AeroDR 3 Series in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0510609 and owned by KONICA MINOLTA, INC. The device was registered on April 21, 2025.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

Free Database
Powered by Pure Global AI
HSA Official Data
CLASS B
DE0510609
KONICA MINOLTA AeroDR 3 Series
HSA Registration Number: DE0510609
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Description

SKR 3000 is intended to image the X-ray transmitted through the human body by an X-ray flat panel detector, and to output an X-ray Image. The X-ray image does not include any mammographic image.

Device Classification
Device Class
CLASS B
Medical Speciality Area
Radiology / Imaging
Registration Information
Registration Number
DE0510609
Registration Date
April 21, 2025
Retention Due Date
April 20, 2026
Product Owner
Short Name
KONICA MINOLTA, INC
Address
1 Sakura-machi,, Hino-shi, Tokyo,, 191-8511 Japan, JAPAN
Registrant
Address
79 SCIENCE PARK DRIVE, CINTECH IV, #02-01/08, SINGAPORE 118264
Importer
Address
196 PANDAN LOOP, PANTECH BUSINESS HUB, #04-29, SINGAPORE 128384 196 PANDAN LOOP, PANTECH BUSINESS HUB, #04-29, SINGAPORE 128384 79 SCIENCE PARK DRIVE, CINTECH IV, #02-01, SINGAPORE 118264
Model Information
Model Name(s)
AeroDR 3 1417HD2 AeroDR 3 1717HD2 AeroDR 3 1417SL AeroDR 3 1417HL AeroDR 3 1717HL
Model Identifier(s)
P-65 P-75 P-82 P-85 P-95