Taiwan FDA registration b2f4e9c66ef27968160fd74d1f8d4cde

"HONHI" Dental Hand Instrument (Non-Sterile)

TW: "鴻海" 牙科手用器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·E. HAHNENKRATT GMBH·Registered Feb 12, 2010 – Feb 12, 2025Expired
Registration details
Analysis ID
b2f4e9c66ef27968160fd74d1f8d4cde
License Form
Department of Health Medical Device Import No. 008539
Customs Code
DHA04400853902
Company information
Manufacturer Country
Germany
Authorized Representative
HONHI MEDICAL CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F4565 Hand instruments for dental use
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 12, 2010
Expiry Date
Feb 12, 2025
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About this record

Access comprehensive regulatory information for "HONHI" 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 b2f4e9c66ef27968160fd74d1f8d4cde and manufactured by E. HAHNENKRATT GMBH. The authorized representative in Taiwan is HONHI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SHUFA DENTAL CO., MEDFLAIR INSTRUMENTS COMPANY, and 2 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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