Taiwan FDA registration 1bdec08ed43baf83ec36fbf6ee5a7a04

"Renfert" Dental Impression Materials Mixer (Non-Sterile)

TW: "樂福" 印模材自動混合機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RENFERT GMBH·Registered Dec 02, 2020 – Dec 02, 2025Expired
Registration details
Analysis ID
1bdec08ed43baf83ec36fbf6ee5a7a04
License Form
Ministry of Health Medical Device Import No. 022150
Customs Code
DHA09402215001
Company information
Manufacturer
RENFERT GMBH
Manufacturer Country
Germany
Product details
Intended Use
Limited to the first level identification range of dental and mercury instruments (F.3100) in the management of medical devices.
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F3100 Dental and mercury ware
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 02, 2020
Expiry Date
Dec 02, 2025
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About this record

Access comprehensive regulatory information for "Renfert" Dental Impression Materials Mixer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1bdec08ed43baf83ec36fbf6ee5a7a04 and manufactured by RENFERT GMBH. The authorized representative in Taiwan is UNITED MEDICAL SPECIALTIES CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RENFERT GMBH, and 1 recent registrations in the same category. 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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