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"Rebingel" endoscope frontal fixation system - Taiwan Registration 3a6cb5270b5fbc0d2de1132edc9fd498

Access comprehensive regulatory information for "Rebingel" endoscope frontal fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a6cb5270b5fbc0d2de1132edc9fd498 and manufactured by STRYKER LEIBINGER GMBH & CO. KG. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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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3a6cb5270b5fbc0d2de1132edc9fd498
Registration Details
Taiwan FDA Registration: 3a6cb5270b5fbc0d2de1132edc9fd498
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Device Details

"Rebingel" endoscope frontal fixation system
TW: "้›ท่ณ“ๆ ผ็ˆพ" ๅ…ง่ฆ–้ก้ก้ขๅ›บๅฎš็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

3a6cb5270b5fbc0d2de1132edc9fd498

DHA00600951308

Company Information

Product Details

N000 Orthopedics

import

Dates and Status

Sep 28, 2000

Sep 28, 2015

Apr 25, 2018

Cancellation Information

Logged out

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