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Inflatable fracture fixator (unsterilized) - Taiwan Registration 211082b08460e6678ad74e9a91d32ef2

Access comprehensive regulatory information for Inflatable fracture fixator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 211082b08460e6678ad74e9a91d32ef2 and manufactured by HARTWELL MEDICAL CORPORATION. The authorized representative in Taiwan is FU SHING MEDICAL 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.

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211082b08460e6678ad74e9a91d32ef2
Registration Details
Taiwan FDA Registration: 211082b08460e6678ad74e9a91d32ef2
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Device Details

Inflatable fracture fixator (unsterilized)
TW: ๆŠฝๅ……ๆฐฃๅผ้ชจๆŠ˜ๅ›บๅฎšๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

211082b08460e6678ad74e9a91d32ef2

DHA04400369402

Company Information

United States

Product Details

Limited to the first level recognition range of medical equipment management measures for splints for inflated limbs (I.3900).

I General, Plastic Surgery and Dermatology

I.3900 Clamp board for bulging limbs

import

Dates and Status

Apr 12, 2006

Apr 12, 2016

May 17, 2018

Cancellation Information

Logged out

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