Taiwan FDA registration 42ed239bf07dce5fdba28564e2f63b09
"Vock" diagnostic concentrating lenses
TW: "伏克"診斷用聚光鏡片
Registration details
- Analysis ID
- 42ed239bf07dce5fdba28564e2f63b09
- Customs Code
- DHA04400120401
Company information
- Manufacturer
- VOLK OPTICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- Indirect eye examination for binocular use, which produces a direct magnified image of the eye that is inverted or reversed.
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Oct 25, 2005
- Expiry Date
- Oct 25, 2010
- Cancellation Date
- Nov 09, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Vock" diagnostic concentrating lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42ed239bf07dce5fdba28564e2f63b09 and manufactured by VOLK OPTICAL INC.. The authorized representative in Taiwan is CLINICO 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.
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