Pure Global

"Arthroscopy" arthroscopy and its accessories - Taiwan Registration 283621279eab13cde3a6f9f638d2cd6f

Access comprehensive regulatory information for "Arthroscopy" arthroscopy and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 283621279eab13cde3a6f9f638d2cd6f and manufactured by AESCULAP AG. The authorized representative in Taiwan is Taiwan Birlanc 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
283621279eab13cde3a6f9f638d2cd6f
Registration Details
Taiwan FDA Registration: 283621279eab13cde3a6f9f638d2cd6f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Arthroscopy" arthroscopy and its accessories
TW: "้›…ๆฐ" ้—œ็ฏ€้กๅŠๅ…ถ้™„ไปถ
Risk Class 2
Cancelled

Registration Details

283621279eab13cde3a6f9f638d2cd6f

DHA00601370700

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

import

Dates and Status

Nov 29, 2005

Nov 29, 2020

Jul 15, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€