Taiwan FDA registration b7dac7c27ac9a8ed7f7fb7693ef00fa4

"iEZ" Endosseous Dental Implant Accessories (Non-Sterile) 。

TW: "艾易力"牙齒骨內植入物附件(未滅菌) 。

Taiwan·Risk Class 1·MD·QIN CHUANG PRECISION TECHNOLOGY CO., LTD.·Registered May 04, 2018 – May 04, 2028Active

Registration details

Analysis ID: b7dac7c27ac9a8ed7f7fb7693ef00fa4
License Form: Ministry of Health Medical Device Manufacturing No. 007239

Company information

Manufacturer: QIN CHUANG PRECISION TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: QIN CHUANG PRECISION TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3980 Dental Intraosseous Implant Attachment
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 04, 2018
Expiry Date: May 04, 2028

About this record

Access comprehensive regulatory information for "iEZ" Endosseous Dental Implant Accessories (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 b7dac7c27ac9a8ed7f7fb7693ef00fa4 and manufactured by QIN CHUANG PRECISION TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is QIN CHUANG PRECISION TECHNOLOGY 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.