Pure Global

BIONOX Injectable Artificial Bone Filler Dispenser Set (Sterilized) - Taiwan Registration 4a8389a4deeb5ff746368fb01b34b081

Access comprehensive regulatory information for BIONOX Injectable Artificial Bone Filler Dispenser Set (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4a8389a4deeb5ff746368fb01b34b081 and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
4a8389a4deeb5ff746368fb01b34b081
Registration Details
Taiwan FDA Registration: 4a8389a4deeb5ff746368fb01b34b081
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

BIONOX Injectable Artificial Bone Filler Dispenser Set (Sterilized)
TW: ไฟ่ซพๅฃซ ๅฏๆณจๅฐ„ๅž‹ไบบๅทฅ้ชจๅกซๅ……็‰ฉๅˆ†้…ๅ™จ็ต„ (ๆป…่Œ)
Risk Class 1

Registration Details

4a8389a4deeb5ff746368fb01b34b081

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management measures of medical equipment "Bone cement dispenser (N.4200) first level identification range.

N Orthopedics

N.4200 Bone cement distributor

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Mar 28, 2016

Mar 28, 2026