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“maxmore” spine Endoscopes - Taiwan Registration d1c258262854df084075ddbf49045273

Access comprehensive regulatory information for “maxmore” spine Endoscopes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d1c258262854df084075ddbf49045273 and manufactured by HOOGLAND SPINE PRODUCTS GMBH. The authorized representative in Taiwan is CHIN I PAO CO., LTD..

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d1c258262854df084075ddbf49045273
Registration Details
Taiwan FDA Registration: d1c258262854df084075ddbf49045273
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Device Details

“maxmore” spine Endoscopes
TW: “麥克斯摩爾”脊椎內視鏡
Risk Class 2
MD

Registration Details

d1c258262854df084075ddbf49045273

Ministry of Health Medical Device Import No. 033642

DHA05603364200

Company Information

Germany

Product Details

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

N Orthopedic devices

N1100 Arthroscopy

Imported from abroad

Dates and Status

May 16, 2020

May 16, 2025