Taiwan FDA registration f68bfa1d679c471b6e76808371046975
Endi Otoscopes (Unsterilized)
TW: 恩帝 耳鏡專用耳套 (未滅菌)
Taiwan·Risk Class 1·DI CHENG RUBBER INDUSTRIES INC.·Registered Apr 12, 2013 – Apr 12, 2023ExpiredRegistration details
- Analysis ID
- f68bfa1d679c471b6e76808371046975
Company information
- Manufacturer
- DI CHENG RUBBER INDUSTRIES INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- APPLE BIOMEDICAL INC.
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
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Apr 12, 2013
- Expiry Date
- Apr 12, 2023
About this record
Access comprehensive regulatory information for Endi Otoscopes (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f68bfa1d679c471b6e76808371046975 and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is APPLE BIOMEDICAL INC..
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