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"Bayer Janice" bone explant system - Taiwan Registration 57fda29ee698c0b8281fd5225a30ea83

Access comprehensive regulatory information for "Bayer Janice" bone explant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 57fda29ee698c0b8281fd5225a30ea83 and manufactured by BIOGENESIS CO., LTD.. The authorized representative in Taiwan is DENMAX CORPORATION.

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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57fda29ee698c0b8281fd5225a30ea83
Registration Details
Taiwan FDA Registration: 57fda29ee698c0b8281fd5225a30ea83
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Device Details

"Bayer Janice" bone explant system
TW: โ€œๆ‹œ่€ณ็ๅฆฎ็ตฒโ€้ชจๅ…งๆค้ซ”็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

57fda29ee698c0b8281fd5225a30ea83

DHA00602371502

Company Information

Korea, Republic of

Product Details

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

F Dentistry

F.3640 Bone Implants

import

Dates and Status

Jul 19, 2012

Jul 19, 2017

Dec 13, 2019

Cancellation Information

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