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"Sandek" electrosurgical system - Taiwan Registration e9c501c1e5aa9dc8dc51c7882ed0e36c

Access comprehensive regulatory information for "Sandek" electrosurgical system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e9c501c1e5aa9dc8dc51c7882ed0e36c and manufactured by SOMETECH INC.. The authorized representative in Taiwan is MEDWAY BME CORPORATION.

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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e9c501c1e5aa9dc8dc51c7882ed0e36c
Registration Details
Taiwan FDA Registration: e9c501c1e5aa9dc8dc51c7882ed0e36c
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Device Details

"Sandek" electrosurgical system
TW: โ€œๆก‘ๅพทๅ…‹โ€้›ปๅˆ€็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

e9c501c1e5aa9dc8dc51c7882ed0e36c

DHA00602361307

Company Information

Korea, Republic of

Product Details

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

I General, Plastic Surgery and Dermatology

I.4400 Cutting and hemostasis electric knives and accessories thereof

import

Dates and Status

Jun 07, 2012

Jun 07, 2017

Nov 26, 2019

Cancellation Information

Logged out

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