Taiwan FDA registration e64729c758dd2ef2936ce6d9b295410c
Phonak Air Guided Hearing Aids (Unsterilized)
TW: "瑞士峰力" 氣導式助聽器 (未滅菌)
Registration details
- Analysis ID
- e64729c758dd2ef2936ce6d9b295410c
- Customs Code
- DHA09600356602
Company information
- Manufacturer
- SONOVA HEARING (SUZHOU) CO. LTD.
- Manufacturer Country
- China
- Authorized Representative
- SONOVA TAIWAN PTE LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the classification and grading management measures for medical devices "hearing aids (G.3300)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Sep 27, 2018
- Expiry Date
- Sep 27, 2028
About this record
Access comprehensive regulatory information for Phonak Air Guided Hearing Aids (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e64729c758dd2ef2936ce6d9b295410c and manufactured by SONOVA HEARING (SUZHOU) CO. LTD.. The authorized representative in Taiwan is SONOVA TAIWAN PTE 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.
Free DatabasePowered by Pure Global AI89,000+ Devices