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"Ian Ripple" powered therapy unit (unsterilized) - Taiwan Registration 766977a5c1a4cdb7faf2d0f9c6dafe9b

Access comprehensive regulatory information for "Ian Ripple" powered therapy unit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 766977a5c1a4cdb7faf2d0f9c6dafe9b and manufactured by ENRAF-NONIUS B.V.. The authorized representative in Taiwan is Jiatai Medical Equipment Co., 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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766977a5c1a4cdb7faf2d0f9c6dafe9b
Registration Details
Taiwan FDA Registration: 766977a5c1a4cdb7faf2d0f9c6dafe9b
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Device Details

"Ian Ripple" powered therapy unit (unsterilized)
TW: "ไผŠๆฉ็‘ž็ฆ" ๅ‹•ๅŠ›ๅผๆฒป็™‚ๆชฏ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

766977a5c1a4cdb7faf2d0f9c6dafe9b

DHA04400997208

Company Information

Netherlands

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Isokinetic Muscle Strength Test Evaluation System (O.1925)".

o Physical Medical Sciences

O.3760 Powered therapy cage

import

Dates and Status

Mar 02, 2011

Mar 02, 2016

Jun 08, 2018

Cancellation Information

Logged out

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