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"Bayer Janice" bridge system for bone explants - Taiwan Registration e682b780a381cadc51db3c5756c8e54e

Access comprehensive regulatory information for "Bayer Janice" bridge system for bone explants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e682b780a381cadc51db3c5756c8e54e 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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e682b780a381cadc51db3c5756c8e54e
Registration Details
Taiwan FDA Registration: e682b780a381cadc51db3c5756c8e54e
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Device Details

"Bayer Janice" bridge system for bone explants
TW: โ€œๆ‹œ่€ณ็ๅฆฎ็ตฒโ€้ชจๅ…งๆค้ซ”็”จ็‰™ๆฉ‹็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

e682b780a381cadc51db3c5756c8e54e

DHA00602367302

Company Information

Korea, Republic of

Product Details

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

F Dentistry

F.3630 Bolsters for intraosseous implants

import

Dates and Status

Jun 13, 2012

Jun 13, 2017

Dec 13, 2019

Cancellation Information

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