Taiwan FDA registration 0cd1794ed91647abcd24909092c7a8b9
“T-Rex” Rexton air conduction hearing aid (non-sterile)
TW: “承輝” 雷克斯頓氣導式助聽器 (未滅菌)
Taiwan·Risk Class 1·MD·SIEMENS MEDICAL INSTRUMENTS PTE LTD·Registered Jul 15, 2014 – Jul 15, 2019CancelledRegistration details
- Analysis ID
- 0cd1794ed91647abcd24909092c7a8b9
- License Form
- Ministry of Health Medical Device Import No. 014328
- Customs Code
- DHA09401432807
Company information
- Manufacturer
- SIEMENS MEDICAL INSTRUMENTS PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- T-REX HEARING SPEECH CO., LTD.
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G3300 hearing aid
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 15, 2014
- Expiry Date
- Jul 15, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for “T-Rex” Rexton air conduction hearing aid (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 0cd1794ed91647abcd24909092c7a8b9 and manufactured by SIEMENS MEDICAL INSTRUMENTS PTE LTD. The authorized representative in Taiwan is T-REX HEARING SPEECH 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