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"Deca" three-vitality infrared laser treatment instrument - Taiwan Registration 28ab55db641be5102ff1eab05bf246a0

Access comprehensive regulatory information for "Deca" three-vitality infrared laser treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28ab55db641be5102ff1eab05bf246a0 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is NEOASIA 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.

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28ab55db641be5102ff1eab05bf246a0
Registration Details
Taiwan FDA Registration: 28ab55db641be5102ff1eab05bf246a0
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Device Details

"Deca" three-vitality infrared laser treatment instrument
TW: โ€œๅพทๅกโ€ไธ‰ๆดปๅŠ›็ด…ๅค–็ทš้›ทๅฐ„ๆฒป็™‚ๅ„€
Risk Class 2
Cancelled

Registration Details

28ab55db641be5102ff1eab05bf246a0

DHA00601796704

Company Information

Italy

Product Details

It temporarily improves local blood circulation and relieves muscle pain and stiffness.

I General, Plastic Surgery and Dermatology

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

import

Dates and Status

Mar 28, 2007

Mar 28, 2017

Dec 20, 2019

Cancellation Information

Logged out

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