Pure Global
180190
III
current

Suture Anchors็ผๅˆ้”š

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

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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
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

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Pricing
Manufacturer (่ฃฝ้€ ๅ•†)
Stryker Endoscopy, a Division of Stryker Corporation
Stryker Endoscopy, A Division Of Stryker Corporation
United States
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5900 Optical Court, San Jose, CA 95138, USA
5900ๅ…‰ๅญฆๆณ•้™ข,ๅœฃไฝ•ๅกž,CA 95138,็พŽๅ›ฝ
Authorised Representative (AR)
Stryker China Limited
็พŽๅ›ฝๅฒ่ต›ๅ…‹(ไธญๅ›ฝ)ๆœ‰้™ๅ…ฌๅธ
39691200
Regulatory Timeline
Registration Date
May 23, 2023
Expiry Date
June 21, 2028
Product Models
ProCinch Adjustable Loop Implant (234-102-060, 234-102-090, 234-102-101)
ProCinch ๅฏ่ฐƒ่Š‚็Žฏๅฝขๆคๅ…ฅ็‰ฉ (234-102-060, 234-102-090, 234-102-101)