220171
III
current
Suture Anchors็ผๅ้
This profile provides complete Hong Kong MDACS registration information for Suture Anchors. 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: Suture Anchors
็ขๅ่ณ่จ๏ผ ็ผๅ้
Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
22538
Product Code Detail
22538 Suture Anchors
State
current
Status
N/A
Manufacturer (่ฃฝ้ ๅ)
Biomet Sports Medicine
Biomet Sports Medicine
United States
็พๅฝ
56 East Bell Drive, P.O. Box 587, Warsaw, Indiana, 46581, USA
56 East Bell Drive, P.O. Box 587, ๅๆฒ, ๅฐ็ฌฌๅฎ็บณๅท, 46581, ็พๅฝ
Authorised Representative (AR)
29920968
Regulatory Timeline
Registration Date
June 06, 2024
Expiry Date
June 01, 2027
Product Models
JuggerStitch Meniscal Repair Device, Straight (110024772, 110024772N), JuggerStitch Meniscal Repair Device, Curved (110024773, 110024773N), JuggerStitch Halfpipe Cannula Sled (110027358), JuggerStitch Suture Cutter (110031679)
JuggerStitch ๅๆๆฟไฟฎๅค่ฃ
็ฝฎ,็ดๅผ (110024772, 110024772N), JuggerStitch ๅๆๆฟไฟฎๅค่ฃ
็ฝฎ,ๅผฏๆฒ (110024773, 110024773N), JuggerStitch ๅ็ฎกๆ็ฎก้ชๆฉ (110027358), JuggerStitch ็ผๅๅๅฒๆบ (110031679)