Taiwan FDA registration d85c9b4c243174962c1632ad042115f6

"PINTOLI" Limb Orthosis (Non-Sterile)

TW: "賓特立" 肢體裝具 (未滅菌)

Taiwan·Risk Class 1·MD·PINTOLI ENTERPRISE CO., LTD.·Registered Jun 13, 2017 – Jun 13, 2022Cancelled

Registration details

Analysis ID: d85c9b4c243174962c1632ad042115f6
License Form: Ministry of Health Medical Device Manufacturing No. 006773

Company information

Manufacturer: PINTOLI ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PINTOLI ENTERPRISE CO., LTD.

Product details

Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3475 Body Equipment
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Jun 13, 2017
Expiry Date: Jun 13, 2022

Cancellation information

Status: Logged out
Reason: 轉為登錄字號

About this record

Access comprehensive regulatory information for "PINTOLI" Limb Orthosis (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 d85c9b4c243174962c1632ad042115f6 and manufactured by PINTOLI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is PINTOLI ENTERPRISE 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.