Taiwan FDA registration f57e7f7478e2af83bb51ebdfff1b5cf5

Resir Vicker Pulse and Q-switched ruby laser

TW: 雷斯爾衛長脈衝及Ｑ開關紅寶石雷射

Taiwan·LAMBDA PHOTOMETRICS LTD.·Registered Mar 23, 1998 – Mar 23, 2003Cancelled

Registration details

Analysis ID: f57e7f7478e2af83bb51ebdfff1b5cf5
Customs Code: DHA00600860801

Company information

Manufacturer: LAMBDA PHOTOMETRICS LTD.
Manufacturer Country: United Kingdom
Authorized Representative: Huisheng Enterprise Limited

Product details

Product Type (Level 1): 2100 Medical Laser Unit
Import Information: import

Dates and status

Registration Date: Mar 23, 1998
Expiry Date: Mar 23, 2003
Cancellation Date: Dec 13, 2004

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for Resir Vicker Pulse and Q-switched ruby laser in Taiwan's medical device market through Pure Global AI's free database. is registered under number f57e7f7478e2af83bb51ebdfff1b5cf5 and manufactured by LAMBDA PHOTOMETRICS LTD.. The authorized representative in Taiwan is Huisheng Enterprise Limited.

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.