Pure Global
190424
IV
current

Cartilage biomatrix implant่ฝฏ้ชจ็”Ÿ็‰ฉๅŸบ่ดจๆคๅ…ฅ็‰ฉ

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
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Manufacturer (่ฃฝ้€ ๅ•†)
United States
็พŽๅ›ฝ
150 Minuteman Road, Andover, MA 01810 USA
150ๆฐ‘ๅ…ต่ทฏ,ๅฎ‰ๅคšๅผ—,MA 01810 ็พŽๅ›ฝ
Authorised Representative (AR)
Smith & Nephew Limited
ๆ–ฝไน่พ‰ๆœ‰้™ๅ…ฌๅธ
26487700
Regulatory Timeline
Registration Date
January 24, 2020
Expiry Date
January 24, 2025
Product Models
CARGEL Bioscaffold (72204980)
ๅกๆ ผๅฐ”็”Ÿ็‰ฉๆ”ฏๆžถ (72204980)