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“WAVE PEP”Dental Hand Instrument (Non-sterile) - Taiwan Registration 2af76d32d73dc4d337d8efdd9d5fc32e

Access comprehensive regulatory information for “WAVE PEP”Dental Hand Instrument (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 2af76d32d73dc4d337d8efdd9d5fc32e and manufactured by FRANK DENTAL GMBH. The authorized representative in Taiwan is WAVE PEP TRADE CO., LTD..

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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2af76d32d73dc4d337d8efdd9d5fc32e
Registration Details
Taiwan FDA Registration: 2af76d32d73dc4d337d8efdd9d5fc32e
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Device Details

“WAVE PEP”Dental Hand Instrument (Non-sterile)
TW: “偉平”牙科手用器械 (未滅菌)
Risk Class 1
MD

Registration Details

2af76d32d73dc4d337d8efdd9d5fc32e

Ministry of Health Medical Device Import No. 022642

DHA09402264209

Company Information

Germany

Product Details

Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

Sep 09, 2021

Sep 09, 2026