Taiwan FDA registration bc9af132f9e713998e052a0726c0d24d

"Riester" Magnifying Loupes and Accessories (Non-Sterile)

TW: "瑞司" 放大鏡及其附件 (未滅菌)

Taiwan·Risk Class 1·MD·Rudolf Riester GmbH·Registered May 19, 2017 – May 19, 2027Active

Registration details

Analysis ID: bc9af132f9e713998e052a0726c0d24d
License Form: Ministry of Health Medical Device Import No. 017861
Customs Code: DHA09401786101

Company information

Manufacturer: Rudolf Riester GmbH
Manufacturer Country: Germany
Authorized Representative: BOYANG MEDICAL TECHNOLOGY CO., LTD

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: May 19, 2017
Expiry Date: May 19, 2027

About this record

Access comprehensive regulatory information for "Riester" Magnifying Loupes and 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 bc9af132f9e713998e052a0726c0d24d and manufactured by Rudolf Riester GmbH. The authorized representative in Taiwan is BOYANG MEDICAL 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.