Taiwan FDA registration 2baf233e0b01119f6d0bc1aed90d0c85

"B&L" Endodontic Root Canal Plugger (Non-Sterile)

TW: "碧艾樂" 根管充填器 (未滅菌)

Taiwan·Risk Class 1·MD·B&L BIOTECH INC.·Registered Sep 15, 2020 – Sep 15, 2025Expired

Registration details

Analysis ID: 2baf233e0b01119f6d0bc1aed90d0c85
License Form: Ministry of Health Medical Device Import No. 021964
Customs Code: DHA09402196400

Company information

Manufacturer: B&L BIOTECH INC.
Manufacturer Country: Korea, Republic of
Authorized Representative: ASIANTOP ENTERPRISE 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: Sep 15, 2020
Expiry Date: Sep 15, 2025

About this record

Access comprehensive regulatory information for "B&L" Endodontic Root Canal Plugger (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 2baf233e0b01119f6d0bc1aed90d0c85 and manufactured by B&L BIOTECH INC.. The authorized representative in Taiwan is ASIANTOP ENTERPRISE CO., LTD..

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