Taiwan FDA registration 72469e0a5d16ffdafa5b153e1b3ebc96

"KNEESUP Care" Goniometer (Non-Sterile)

TW: "安膝" 電子量角器 (未滅菌)

Taiwan·Risk Class 1·MD·K-Lian Intelligent Medical Equipment Co., Ltd·Registered Sep 04, 2019 – Sep 04, 2024Expired

Registration details

Analysis ID: 72469e0a5d16ffdafa5b153e1b3ebc96
License Form: Ministry of Health Medical Device Manufacturing No. 007937

Company information

Manufacturer: K-Lian Intelligent Medical Equipment Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: K-Lian Intelligent Medical Equipment Co., Ltd

Product details

Intended Use: Limited to the first level identification range of the "goniometer (N.1500)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N1500 Angle Meter
Import Information: Produced in Taiwan, China; GMP

Dates and status

Registration Date: Sep 04, 2019
Expiry Date: Sep 04, 2024

About this record

Access comprehensive regulatory information for "KNEESUP Care" Goniometer (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 72469e0a5d16ffdafa5b153e1b3ebc96 and manufactured by K-Lian Intelligent Medical Equipment Co., Ltd. The authorized representative in Taiwan is K-Lian Intelligent Medical Equipment 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.