Pure Global

"Otto Bock" External limb prosthetic component(Non-Sterile) - Taiwan Registration 5791564e18887a35e8320e327e822c1d

Access comprehensive regulatory information for "Otto Bock" External limb prosthetic component(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5791564e18887a35e8320e327e822c1d and manufactured by OTTOBOCK SE & CO. KGAA. The authorized representative in Taiwan is OTTO BOCK ASIA PACIFIC LIMITED TAIWAN BRANCH (H.K.).

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
5791564e18887a35e8320e327e822c1d
Registration Details
Taiwan FDA Registration: 5791564e18887a35e8320e327e822c1d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Otto Bock" External limb prosthetic component(Non-Sterile)
TW: "ๅฅงๆ‰˜ๅšๅ…‹"้ซ”ๅค–่‚ข้ซ”็พฉ่‚ข็”จ็ต„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5791564e18887a35e8320e327e822c1d

Ministry of Health Medical Device Import Registration No. 004096

DHA08400409600

Company Information

Product Details

Limited to the first level recognition range of components for in vitro limb prosthetics (O.3420) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3420 Components for in vitro limb prosthetics

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026