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"Qin Sheng" helium-neon laser - Taiwan Registration 2d9895376c54d9e67ff0ac92d38a7fee

Access comprehensive regulatory information for "Qin Sheng" helium-neon laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2d9895376c54d9e67ff0ac92d38a7fee and manufactured by NEEDLELESS CORPORATION. The authorized representative in Taiwan is Jin-Cheng Medical Company 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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2d9895376c54d9e67ff0ac92d38a7fee
Registration Details
Taiwan FDA Registration: 2d9895376c54d9e67ff0ac92d38a7fee
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Device Details

"Qin Sheng" helium-neon laser
TW: โ€œ่ฆฒๆ™Ÿโ€ๆฐฆๆฐ–้›ทๅฐ„
Risk Class 2

Registration Details

2d9895376c54d9e67ff0ac92d38a7fee

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

Contract manufacturing;; Domestic

Dates and Status

Mar 16, 2022

Mar 16, 2027