Taiwan FDA registration 5a02d1d7cc2c947a2795f418c681acfb

"B&E" Endosseous dental implant accessories (Non-Sterile)

TW: "賓麗"牙齒骨內植入物附件(未滅菌)

Taiwan·Risk Class 1·MD·B&E KOREA CO., LTD·Registered Oct 03, 2017 – Oct 03, 2022Expired

Registration details

Analysis ID: 5a02d1d7cc2c947a2795f418c681acfb
License Form: Ministry of Health Medical Device Import No. 018377
Customs Code: DHA09401837701

Company information

Manufacturer: B&E KOREA CO., LTD
Manufacturer Country: Korea, Republic of
Authorized Representative: CHENG WEI BIOTECH 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: Imported from abroad

Dates and status

Registration Date: Oct 03, 2017
Expiry Date: Oct 03, 2022

About this record

Access comprehensive regulatory information for "B&E" 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 5a02d1d7cc2c947a2795f418c681acfb and manufactured by B&E KOREA CO., LTD. The authorized representative in Taiwan is CHENG WEI BIOTECH 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.