Pure Global

"Medtronic" craniomaxillofacial fixation system - Taiwan Registration 816b82d99da8beba50276dc1aea0cfa5

Access comprehensive regulatory information for "Medtronic" craniomaxillofacial fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 816b82d99da8beba50276dc1aea0cfa5 and manufactured by MEDTRONIC NEUROSURGERY. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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
816b82d99da8beba50276dc1aea0cfa5
Registration Details
Taiwan FDA Registration: 816b82d99da8beba50276dc1aea0cfa5
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medtronic" craniomaxillofacial fixation system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€้กฑ้ œ้ขๅ›บๅฎš็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

816b82d99da8beba50276dc1aea0cfa5

DHA00601801404

Company Information

United States

Product Details

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

N Orthopedics

N.3030 Single or multiple metallic bone fixation devices and accessories

import

Dates and Status

Apr 13, 2007

Apr 13, 2017

Dec 13, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ