Taiwan FDA registration b313c721dc57162eaaa7ee90d034b39d
ZEISS Henfrey Vision Analyzer II-I Series (Unsterilized)
TW: 蔡司韓福瑞視野分析儀II-I系列 (未滅菌)
Taiwan·Risk Class 1·CARL ZEISS MEDITEC, INC.·Registered Oct 17, 2005 – Oct 17, 2020CancelledRegistration details
- Analysis ID
- b313c721dc57162eaaa7ee90d034b39d
- Customs Code
- DHA04400096607
Company information
- Manufacturer
- CARL ZEISS MEDITEC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TAIWAN INSTRUMENT CO., LTD.
Product details
- Intended Use
- Used to check the extent of the patient's peripheral vision. The device casts different points of light on the surface and allows the patient to indicate whether they can see the light or not.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1605 Periscope
- Import Information
- import
Dates and status
- Registration Date
- Oct 17, 2005
- Expiry Date
- Oct 17, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for ZEISS Henfrey Vision Analyzer II-I Series (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b313c721dc57162eaaa7ee90d034b39d and manufactured by CARL ZEISS MEDITEC, INC.. The authorized representative in Taiwan is TAIWAN INSTRUMENT 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