110418
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
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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
Manufacturer (่ฃฝ้ ๅ)
Smith & Nephew Inc.
Smith+Nephew
United States
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Endoscopy, 150 Minuteman Road, Andover, Massachusetts 01810-1031, USA
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็ชฅ้ๆฃๆฅ, 150 Minuteman Road, Andover, Massachusetts 01810-1031, USA
Authorised Representative (AR)
Smith & Nephew Limited
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26487700
Regulatory Timeline
Registration Date
July 24, 2024
Expiry Date
November 18, 2026
Product Models
Footprint Ultra PK Suture Anchor (72202901, 72202902)
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PK็ผๅ้ๆ (72202901,72202902)