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"Enrif" electrotherapy device - Taiwan Registration e4c645e79663c21df261d712ae33bfdb

Access comprehensive regulatory information for "Enrif" electrotherapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4c645e79663c21df261d712ae33bfdb and manufactured by ENRAF-NONIUS B.V.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.

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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e4c645e79663c21df261d712ae33bfdb
Registration Details
Taiwan FDA Registration: e4c645e79663c21df261d712ae33bfdb
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Device Details

"Enrif" electrotherapy device
TW: โ€œๆฉ็‘ž็ฆโ€้›ป็™‚ๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

e4c645e79663c21df261d712ae33bfdb

DHA00601891108

Company Information

Netherlands

Product Details

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

o Physical Medical Sciences

O.5850 5850.

import

Dates and Status

Jun 18, 2008

Jun 18, 2023