Pure Global
190032
III
current

Orthopedic Cement้ชจ็ง‘ๆฐดๆณฅ

This profile provides complete Hong Kong MDACS registration information for Orthopedic Cement. 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: Orthopedic Cement

็”ขๅ“่ณ‡่จŠ๏ผš ้ชจ็ง‘ๆฐดๆณฅ

Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
12830
Product Code Detail
12830 Orthopedic Cement
State
current
Status
N/A
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

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Manufacturer (่ฃฝ้€ ๅ•†)
Stryker Instruments, a Division of Stryker Corporation
Stryker Instruments, A Division Of Stryker Corporation
United States
็พŽๅ›ฝ
4100 East Milham Avenue, Kalamazoo MI 49001-6797, USA
4100ไธœ็ฑณๅ‹’ๅง†ๅคง้“,ๅกๆ‹‰้ฉฌ็ฅ–MI 49001-6797,็พŽๅ›ฝ
Authorised Representative (AR)
Stryker China Limited
็พŽๅ›ฝๅฒ่ต›ๅ…‹(ไธญๅ›ฝ)ๆœ‰้™ๅ…ฌๅธ
39691200
Regulatory Timeline
Registration Date
December 08, 2023
Expiry Date
January 24, 2029
Product Models
Spineplex Dual Pack (0406-222-000), VertaPlex Dual Pack (0406-422-000), VertaPlex HV (0406-622-015), VertaPlex HV Dual Pack (0406-622-000), PCD with VertaPlex HV Kit (0507-589-000), Autoplex System without Needles with VertaPlex HV Bone Cement (0607-687-000), PCD Prec. System Long Tube W/VertaPlex HV (0507-586-000)
่„ŠๆŸฑๅŒๅŒ… (0406-222-000), VertaPlex ๅŒๅŒ… (0406-422-000), VertaPlex ้ซ˜ๅŽ‹ (0406-622-015), VertaPlex ้ซ˜ๅŽ‹ๅŒ็ป„ (0406-622-000), ๅธฆ VertaPlex ้ซ˜ๅŽ‹ๅฅ—ไปถ็š„ PCD (0507-589-000), ๅธฆ VertaPlex ้ซ˜ๅŽ‹้ชจๆฐดๆณฅ็š„ๆ— ้’ˆ่‡ชๅŠจๅคๅˆ็ณป็ปŸ (0607-687-000), PCD ้ข„็ณป็ปŸ้•ฟ็ฎกๅธฆ VertaPlex ้ซ˜ๅŽ‹ (0507-586-000)