190424
IV
current
Cartilage biomatrix implant่ฝฏ้ชจ็็ฉๅบ่ดจๆคๅ ฅ็ฉ
This profile provides complete Hong Kong MDACS registration information for Cartilage biomatrix implant. 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.
Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
IV
Product Code
N/A
State
current
Status
N/A
Manufacturer (่ฃฝ้ ๅ)
Smith & Nephew, Inc.
Smith+Nephew
United States
็พๅฝ
150 Minuteman Road, Andover, MA 01810 USA
150ๆฐๅ
ต่ทฏ,ๅฎๅคๅผ,MA 01810 ็พๅฝ
Authorised Representative (AR)
Smith & Nephew Limited
ๆฝไน่พๆ้ๅ
ฌๅธ
26487700
Regulatory Timeline
Registration Date
January 24, 2020
Expiry Date
January 24, 2025
Product Models
CARGEL Bioscaffold (72204980)
ๅกๆ ผๅฐ็็ฉๆฏๆถ (72204980)

