Taiwan FDA registration efc2d739a727ccc9f21b28b11f67dacc
"Rester" otoscopes and their accessories (unsterilized)
TW: "瑞斯特" 耳鏡及其附件 (未滅菌)
Registration details
- Analysis ID
- efc2d739a727ccc9f21b28b11f67dacc
- Customs Code
- DHA04401084705
Company information
- Manufacturer
- RUDOLF RIESTER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- XIN BO ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4770 Ear Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Sep 16, 2011
- Expiry Date
- Sep 16, 2016
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Rester" otoscopes and their accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number efc2d739a727ccc9f21b28b11f67dacc and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is XIN BO ENTERPRISE 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