Taiwan FDA registration d1317829e6d023437d750107f801e501

"REDA" Gynecologic laparoscope accessories (Non-Sterile)

TW: "鐳鐽" 婦產科用腹腔鏡附件 (未滅菌)

Taiwan·Risk Class 1·MD·REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD·Registered May 16, 2019 – May 16, 2024Expired

Registration details

Analysis ID: d1317829e6d023437d750107f801e501
License Form: Ministry of Health Medical Device Import No. 020452
Customs Code: DHA09402045207

Company information

Manufacturer: REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD
Manufacturer Country: Singapore
Authorized Representative: Medical Dragon Ltd.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Laparoscopy and Its Accessories for Obstetrics and Gynecology (L.1720)".
Product Type (Level 1): l Devices for obstetrics and gynecology
Product Type (Level 2): L1720 Laparoscopy for obstetrics and gynecology and its accessories
Import Information: Imported from abroad

Dates and status

Registration Date: May 16, 2019
Expiry Date: May 16, 2024

About this record

Access comprehensive regulatory information for "REDA" Gynecologic laparoscope 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 d1317829e6d023437d750107f801e501 and manufactured by REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD. The authorized representative in Taiwan is Medical Dragon 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.