Taiwan FDA registration a71f9630928d5cfd3f25cda5272b0e59

"LANDANGER" Manual Surgical Instruments For General Use (Non-Sterile)

TW: "藍登格" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·LANDANGER·Registered Jan 16, 2020 – Jan 16, 2025Expired

Registration details

Analysis ID: a71f9630928d5cfd3f25cda5272b0e59
License Form: Ministry of Health Medical Device Import No. 021197
Customs Code: DHA09402119709

Company information

Manufacturer: LANDANGER
Manufacturer Country: France
Authorized Representative: EVOLUTION WORLDWIDE 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: Jan 16, 2020
Expiry Date: Jan 16, 2025

About this record

Access comprehensive regulatory information for "LANDANGER" Manual Surgical Instruments For General Use (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 a71f9630928d5cfd3f25cda5272b0e59 and manufactured by LANDANGER. The authorized representative in Taiwan is EVOLUTION WORLDWIDE 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.