230118
II
current
Curettes, Biopsy, Bronchus, Endoscopic, Flexibleๅฎๅ,ๆดปๆฃ,ๆฏๆฐ็ฎก,ๅ ็ชฅ้,ๆๆง
This profile provides complete Hong Kong MDACS registration information for Curettes, Biopsy, Bronchus, Endoscopic, Flexible. Review device classification, authorised representative (AR) details, manufacturer contacts, product codes, and regulatory milestones. Pure Global AI delivers bilingual transparency for medical device registrations across Asia.
Product Info: Curettes, Biopsy, Bronchus, Endoscopic, Flexible
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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
II
Product Code
21310
Product Code Detail
21310 Curettes, Biopsy, Bronchus, Endoscopic, Flexible
State
current
Status
N/A
Manufacturer (่ฃฝ้ ๅ)
Japan
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2951 Ishikawa-cho, Hachioji-shi, Tokyo, 192-8507 Japan
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Authorised Representative (AR)
Regulatory Timeline
Registration Date
April 06, 2023
Expiry Date
April 06, 2028
Product Models
Single Use Guiding Device (CC-220DR)
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็ฝฎ (CC-220DR)