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"DORNIER" orthopedic extracorporeal shock wave therapy instrument - Taiwan Registration 225eb0d4124ca2d2fa4ad58ef85bffb1

Access comprehensive regulatory information for "DORNIER" orthopedic extracorporeal shock wave therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 225eb0d4124ca2d2fa4ad58ef85bffb1 and manufactured by Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..

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225eb0d4124ca2d2fa4ad58ef85bffb1
Registration Details
Taiwan FDA Registration: 225eb0d4124ca2d2fa4ad58ef85bffb1
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Device Details

"DORNIER" orthopedic extracorporeal shock wave therapy instrument
TW: โ€œๅคšๅฐผ็ˆพโ€้ชจ็ง‘้ซ”ๅค–้œ‡ๆณขๆฒป็™‚ๅ„€
Risk Class 3

Registration Details

225eb0d4124ca2d2fa4ad58ef85bffb1

DHA00601809007

Company Information

Product Details

CALCIFIED TENDONITIS-่‚ฉ้ˆฃๅŒ–ๆ€งๆˆ–้ž้ˆฃๅŒ–ๆ€ง่‚Œ่…ฑ็‚Ž,EPICONDYLITIS (TENNIS AND GOLF ELBOW)-่‚˜ไธŠ้ซ็‚Ž(็ถฒ็ƒ่‚˜),PLANTAR FASCIITIS (HEEL SPUR)-่ถณๅบ•็ญ‹่†œ็‚Ž(่…ณ่ธ้ชจๅˆบ),PSEUDARTHROSIS (NON-UNIONS)-้ชจๆŠ˜ๆ„ˆๅˆไธๅ…จ(ๅ‡ๆ€ง้—œ็ฏ€็—‡).

N Orthopedics

N.0001 ้ชจ็ง‘็”จ้ซ”ๅค–้œ‡ๆณข็ณป็ตฑ

import

Dates and Status

May 21, 2007

May 21, 2027