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"Otto Bock"External limb orthotic component(Non-Sterile) - Taiwan Registration a611af1410d0b9cee3d225af74178844

Access comprehensive regulatory information for "Otto Bock"External limb orthotic 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 a611af1410d0b9cee3d225af74178844 and manufactured by OTTOBOCK SE & CO. KGAA. The authorized representative in Taiwan is OTTO BOCK ASIA PACIFIC LIMITED TAIWAN BRANCH (H.K.).

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a611af1410d0b9cee3d225af74178844
Registration Details
Taiwan FDA Registration: a611af1410d0b9cee3d225af74178844
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Device Details

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

Registration Details

a611af1410d0b9cee3d225af74178844

Ministry of Health Medical Device Import Registration No. 004097

DHA08400409702

Company Information

Product Details

Limited to the first-level identification range of components for external limb equipment (O.3410) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3410 Components for external limb devices

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026