Taiwan FDA registration 17170b2a5b96036eacdcdd1774ad95c8

"Heinion" otoscopy (unsterilized)

TW: “海尼恩”耳鏡(未滅菌)

Taiwan·Risk Class 1·HEINE OPTOTECHNIK GMBH & CO. KG·Registered Apr 11, 2008 – Apr 11, 2028Active

Registration details

Analysis ID: 17170b2a5b96036eacdcdd1774ad95c8
Customs Code: DHA04400665405

Company information

Manufacturer: HEINE OPTOTECHNIK GMBH & CO. KG
Manufacturer Country: Germany
Authorized Representative: DENSO SCIENTIFIC CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "Otoscope (G.4770)" of the Administrative Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4770 Ear Mirrors
Import Information: import

Dates and status

Registration Date: Apr 11, 2008
Expiry Date: Apr 11, 2028

About this record

Access comprehensive regulatory information for "Heinion" otoscopy (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 17170b2a5b96036eacdcdd1774ad95c8 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is DENSO SCIENTIFIC 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.