Taiwan FDA registration e865b0acada0778a020d63e4c2d4a20b
"Siemens" Radiant air-guided hearing aids (unsterilized)
TW: “西門子”瑞而聰氣導式助聽器 （未滅菌）
Taiwan·Risk Class 1·SIEMENS MEDICAL INSTRUMENTS PTE LTD·Registered May 07, 2007 – May 07, 2012CancelledRegistration details
- Analysis ID
- e865b0acada0778a020d63e4c2d4a20b
- Customs Code
- DHA04400582705
Company information
- Manufacturer
- SIEMENS MEDICAL INSTRUMENTS PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- Fuling Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- import
Dates and status
- Registration Date
- May 07, 2007
- Expiry Date
- May 07, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siemens" Radiant 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 e865b0acada0778a020d63e4c2d4a20b and manufactured by SIEMENS MEDICAL INSTRUMENTS PTE LTD. The authorized representative in Taiwan is Fuling 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.
Free DatabasePowered by Pure Global AI89,000+ Devices