Taiwan FDA registration 426db0819bf6c6f26413ab4d07d965a3
"Nagashima" otolaryngology treatment chair
TW: "永島" 耳鼻喉科治療椅
Taiwan·Risk Class 1·NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.·Registered Nov 21, 2005 – Nov 21, 2010CancelledRegistration details
- Analysis ID
- 426db0819bf6c6f26413ab4d07d965a3
- Customs Code
- DHA04400204805
Company information
- Manufacturer
- NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- FU TAI TRADING CO., LTD.
Product details
- Intended Use
- It is used to support the patient's specific posture for examination and treatment during an ear examination.
- Product Type (Level 1)
- G ENT Science
- Import Information
- import
Dates and status
- Registration Date
- Nov 21, 2005
- Expiry Date
- Nov 21, 2010
- Cancellation Date
- Nov 20, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nagashima" otolaryngology treatment chair in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 426db0819bf6c6f26413ab4d07d965a3 and manufactured by NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is FU TAI TRADING 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