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Vonflex Light Impression material - Taiwan Registration 09a6a619b544f492eb8fdff8d44f923f

Access comprehensive regulatory information for Vonflex Light Impression material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09a6a619b544f492eb8fdff8d44f923f and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT 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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09a6a619b544f492eb8fdff8d44f923f
Registration Details
Taiwan FDA Registration: 09a6a619b544f492eb8fdff8d44f923f
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Device Details

Vonflex Light Impression material
TW: ่ฑๆบ–่Š็‰น็‰™็ง‘ๅฐๆจกๆ
Risk Class 2
MD

Registration Details

09a6a619b544f492eb8fdff8d44f923f

Department of Health Medical Device Import No. 023705

DHA00602370502

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F3660 impression material

Imported from abroad

Dates and Status

Jul 09, 2012

Jul 09, 2027