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"Euro Fisther" spinal endoscopy tool (unsterilized) - Taiwan Registration d84121b1d432f7a4c97ecc1b77203e8b

Access comprehensive regulatory information for "Euro Fisther" spinal endoscopy tool (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d84121b1d432f7a4c97ecc1b77203e8b and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is EUROPE ROYAL MEDICAL DEVICES INDUSTRIAL 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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d84121b1d432f7a4c97ecc1b77203e8b
Registration Details
Taiwan FDA Registration: d84121b1d432f7a4c97ecc1b77203e8b
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Device Details

"Euro Fisther" spinal endoscopy tool (unsterilized)
TW: "ๆญๅพก่ฒป็ตฒ็‰น" ่„ŠๆคŽๅ…ง่ฆ–้กๅทฅๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d84121b1d432f7a4c97ecc1b77203e8b

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.

N Orthopedics

N.1100 Closing Lenses

Domestic;; Contract manufacturing

Dates and Status

Jul 04, 2016

Jul 04, 2021

Jun 22, 2022

Cancellation Information

Logged out

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