Pure Global
160189
II
current

Procedure Kit/Trays, Lead Extraction, Pacemaker/Defibrillatorๆ‰‹ๆœฏๅฅ—ไปถ/ๆ‰˜็›˜ใ€ๅฏผ็บฟๆๅ–ใ€่ตทๆๅ™จ/้™ค้ขคๅ™จ

This profile provides complete Hong Kong MDACS registration information for Procedure Kit/Trays, Lead Extraction, Pacemaker/Defibrillator. 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: Procedure Kit/Trays, Lead Extraction, Pacemaker/Defibrillator

็”ขๅ“่ณ‡่จŠ๏ผš ๆ‰‹ๆœฏๅฅ—ไปถ/ๆ‰˜็›˜ใ€ๅฏผ็บฟๆๅ–ใ€่ตทๆๅ™จ/้™ค้ขคๅ™จ

Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
II
Product Code
18111
Product Code Detail
18111 Procedure Kit/Trays, Lead Extraction, Pacemaker/Defibrillator
State
current
Status
N/A
Pure Global
DJ Fang

DJ Fang

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Manufacturer (่ฃฝ้€ ๅ•†)
Spectranetics Corporation
Spectranetics Corporation
United States
็พŽๅ›ฝ
9965 Federal Drive, Colorado Springs, Colorado, 80921, USA
9965่”้‚ฆๅคง้“, ็ง‘็ฝ—ๆ‹‰ๅคšๆ–ฏๆ™ฎๆž—ๆ–ฏ, ็ง‘็ฝ—ๆ‹‰ๅคšๅทž, 80921, ็พŽๅ›ฝ
Authorised Representative (AR)
Innotronik Hong Kong Ltd.
ๆฐธๅˆ›ๅŠ›้ฆ™ๆธฏๆœ‰้™ๅ…ฌๅธ
28776787
Regulatory Timeline
Registration Date
April 07, 2021
Expiry Date
June 21, 2026
Product Models
Lead Locking Device (LLD) 1, 2, 3, E, and EZ and Lead Removal Accessories (518-018, 518-019, 518-020, 518-021, 518-022, 518-023, 518-039, 518-062, 518-067)
ๅผ•็บฟ้”ๅฎš่ฃ…็ฝฎ (LLD) 1ใ€2ใ€3ใ€E ๅ’Œ EZ ไปฅๅŠๅผ•็บฟๅŽป้™ค้™„ไปถ(518-018ใ€518-019ใ€518-020ใ€518-021ใ€518-022ใ€518-023ใ€518-039ใ€518-062ใ€518-067)