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"Emma" excimer therapy device - Taiwan Registration 765989e7c2fa0ecd7142fe3b08145c59

Access comprehensive regulatory information for "Emma" excimer therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 765989e7c2fa0ecd7142fe3b08145c59 and manufactured by Alma Lasers GmbH;; Alma Lasers Ltd.. The authorized representative in Taiwan is GAIA GENOMICS CORP..

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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765989e7c2fa0ecd7142fe3b08145c59
Registration Details
Taiwan FDA Registration: 765989e7c2fa0ecd7142fe3b08145c59
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Device Details

"Emma" excimer therapy device
TW: โ€œ่‰พ็‘ชโ€ๆบ–ๅˆ†ๅญๆฒป็™‚ๅ„€
Risk Class 2
Cancelled

Registration Details

765989e7c2fa0ecd7142fe3b08145c59

DHA05603038201

Company Information

Israel;;Germany

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.4630 ็šฎ่†š็—…็”จ็ดซๅค–็ทš็‡ˆ

import

Dates and Status

Nov 07, 2017

Nov 07, 2022

Apr 12, 2024

Cancellation Information

Logged out

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