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"Schiller" Fred lightweight automatic external defibrillator - Taiwan Registration e91d3a11ff78983504ea113943fa5a5a

Access comprehensive regulatory information for "Schiller" Fred lightweight automatic external defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e91d3a11ff78983504ea113943fa5a5a and manufactured by SCHILLER MEDICAL. The authorized representative in Taiwan is HI-CLEARANCE INC..

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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e91d3a11ff78983504ea113943fa5a5a
Registration Details
Taiwan FDA Registration: e91d3a11ff78983504ea113943fa5a5a
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Device Details

"Schiller" Fred lightweight automatic external defibrillator
TW: โ€œๅธญๅ‹’โ€่ฒป่Šๅพท่ผ•ๅž‹่‡ชๅ‹•้ซ”ๅค–ๅŽป้กซๅ™จ
Risk Class 3

Registration Details

e91d3a11ff78983504ea113943fa5a5a

DHA00602425907

Company Information

France

Product Details

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

E Cardiovascular Medicine Science

E.5310 ่‡ชๅ‹•้ซ”ๅค–ๅŽป้กซๅ™จ็ณป็ตฑ

import

Dates and Status

Dec 14, 2012

Dec 14, 2027