200001
III
current
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This profile provides complete Hong Kong MDACS registration information for Lenses, Intraocular, Posterior Chamber. 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: Lenses, Intraocular, Posterior Chamber
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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
16071
Product Code Detail
16071 Lenses, Intraocular, Posterior Chamber
State
current
Status
N/A
Manufacturer (่ฃฝ้ ๅ)
Johnson & Johnson Surgical Vision, Inc.
Johnson & Johnson Medtech
United States
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31 Technology Drive, Suite 200
Irvine, CA 92618
United States of America
31 Technology Drive,ๅฅๆฟ 200
ๅฐๆนพ, CA 92618
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Authorised Representative (AR)
24803330
Regulatory Timeline
Registration Date
September 22, 2023
Expiry Date
January 30, 2025
Product Models
TECNIS 1-Piece IOL with TECNIS iTec Preloaded Delivery System (PCB00)
TECNIS ไธไฝๅผไบบๅทฅๆถ็ถไฝ,ๅธฆๆณฐๅ
ๅฐผๆฏ iTec ้ขๅ ่ฝฝ่พ้็ณป็ป (PCB00)