Pure Global
90298
IV
Expired.

Catheters, Vascular, Embolectomy/Thrombectomyๅฏผ็ฎกใ€่ก€็ฎกใ€ๆ “ๅกžๅˆ‡้™คๆœฏ/่ก€ๆ “ๅˆ‡้™คๆœฏ

This profile provides complete Hong Kong MDACS registration information for Catheters, Vascular, Embolectomy/Thrombectomy. 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: Catheters, Vascular, Embolectomy/Thrombectomy

็”ขๅ“่ณ‡่จŠ๏ผš ๅฏผ็ฎกใ€่ก€็ฎกใ€ๆ “ๅกžๅˆ‡้™คๆœฏ/่ก€ๆ “ๅˆ‡้™คๆœฏ

Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
IV
Product Code
10714
Product Code Detail
10714 Catheters, Vascular, Embolectomy/Thrombectomy
State
Expired.
Status
N/A
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

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Pricing
Manufacturer (่ฃฝ้€ ๅ•†)
ev3, Inc.
Ev3, Inc.
United States
็พŽๅ›ฝ
3033 Campus Drive, Plymouth, MN 55441, United States
3033ๆ กๅ›ญ้ฉฑๅŠจๅ™จ, ๆ™ฎๅˆฉ่Œ…ๆ–ฏ, MN 55441, ็พŽ
Authorised Representative (AR)
Rapport Medical Science Limited
ๅ‹ๅšๅŒป็–—ๆœ‰้™ๅ…ฌๅธ
37539075
Regulatory Timeline
Registration Date
July 27, 2009
Expiry Date
July 27, 2014
Product Models
SpideRX Embolic Protection Device; SpideFX Embolic Protection Device (SPDRX-030, SPDRX-040, SPDRX-050, SPDRX-060, SPDRX-070, SPD2-030-190, SPD2-040-190, SPD2-050-190, SPD2-060-190, SPD2-070-190, SPD2-030-320, SPD2-040-320, SPD2-050-320, SPD2-060-320, SPD2-070-320)
่œ˜่››็ฝ‘ๆ “ๅกžไฟๆŠค่ฃ…็ฝฎ;SpideFX ๆ “ๅกžไฟๆŠค่ฃ…็ฝฎ (SPDRX-030, SPDRX-040, SPDRX-050, SPDRX-060, SPDRX-070, SPD2-030-190, SPD2-040-190, SPD2-050-190, SPD2-060-190, SPD2-070-190, SPD2-030-320, SPD2-040-320, SPD2-050-320, SPD2-060-320, SPD2-070-320)