90410
II
Delisted.
Cannulae, Intrauterineๅฅ็ฎกใๅฎซๅ
This profile provides complete Hong Kong MDACS registration information for Cannulae, Intrauterine. 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: Cannulae, Intrauterine
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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
II
Product Code
10580
Product Code Detail
10580 Cannulae, Intrauterine
State
Delisted.
Status
N/A
Manufacturer (่ฃฝ้ ๅ)
Ethicon Endo-Surgery, LLC, a Johnson & Johnson Company
Ethicon Endo-Surgery, LLC, a Johnson & Johnson Company
United States
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475 Calle C, Guaynabo, PR 00969, USA
475 Calle C, ็ไผ็บณๆฒ, PR 00969, ็พๅฝ
Authorised Representative (AR)
Johnson & Johnson (Hong Kong) Limited
ๅผบ็ (้ฆๆธฏ) ๆ้ๅ
ฌๅธ
27386080
Regulatory Timeline
Registration Date
October 19, 2009
Expiry Date
October 19, 2014
Product Models
ENDOPATH Uterine Manipulators (UM201, UM202)
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ๅญๅฎซๆ็บตๅจ (UM201, UM202)