Taiwan FDA registration 7db91d3b4b6c1e91f0a5277f88d4f57e

"Danli" torso device (unsterilized)

TW: “丹力”軀幹裝具 (未滅菌)

Taiwan·Risk Class 1·KAO CHEN ENTERPRISE CO., LTD.·Registered Jun 23, 2010 – Jun 23, 2020Cancelled

Registration details

Analysis ID: 7db91d3b4b6c1e91f0a5277f88d4f57e

Company information

Manufacturer: KAO CHEN ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DANIEL DEAR INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.3490 Torso mounting
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Jun 23, 2010
Expiry Date: Jun 23, 2020
Cancellation Date: Jun 22, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Danli" torso device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7db91d3b4b6c1e91f0a5277f88d4f57e and manufactured by KAO CHEN ENTERPRISE CO., LTD.. The authorized representative in Taiwan is DANIEL DEAR INTERNATIONAL 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.