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Resir Vicker Pulse and Q-switched ruby laser - Taiwan Registration f57e7f7478e2af83bb51ebdfff1b5cf5

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.

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f57e7f7478e2af83bb51ebdfff1b5cf5
Registration Details
Taiwan FDA Registration: f57e7f7478e2af83bb51ebdfff1b5cf5
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Device Details

Resir Vicker Pulse and Q-switched ruby laser
TW: ้›ทๆ–ฏ็ˆพ่ก›้•ท่„ˆ่กๅŠ๏ผฑ้–‹้—œ็ด…ๅฏถ็Ÿณ้›ทๅฐ„
Cancelled

Registration Details

f57e7f7478e2af83bb51ebdfff1b5cf5

DHA00600860801

Company Information

United Kingdom

Product Details

2100 Medical Laser Unit

import

Dates and Status

Mar 23, 1998

Mar 23, 2003

Dec 13, 2004

Cancellation Information

Logged out

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