Taiwan FDA registration 07d5031ed0f3e8d853ac598938177f51

"META" EDTA Root Canal Preparator (Non-Sterile)

TW: "麥塔" 根管擴大材 (未滅菌)

Taiwan·Risk Class 1·MD·META BIOMED CO., LTD.·Registered Jun 12, 2020 – Jun 12, 2025Expired

Registration details

Analysis ID: 07d5031ed0f3e8d853ac598938177f51
License Form: Ministry of Health Medical Device Import No. 021632
Customs Code: DHA09402163201

Company information

Manufacturer: META BIOMED CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: UNIGLIFE BIOMED CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4565 Hand instruments for dental use
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 12, 2020
Expiry Date: Jun 12, 2025

About this record

Access comprehensive regulatory information for "META" EDTA Root Canal Preparator (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 07d5031ed0f3e8d853ac598938177f51 and manufactured by META BIOMED CO., LTD.. The authorized representative in Taiwan is UNIGLIFE BIOMED 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.