Taiwan FDA registration 17b4c13cd7ede763f18455cbef5b8d8e
"Costol" tear duct balloon dilation duct
TW: "可思透" 淚管氣球擴張導管
Registration details
- Analysis ID
- 17b4c13cd7ede763f18455cbef5b8d8e
- Customs Code
- DHA04400049405
Company information
- Manufacturer
- QUEST MEDICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- FOCUS MEDICAL INC.
Product details
- Intended Use
- It is used to inflate and widen the obstructed nasal sluggling duct to improve the overflow of tears.
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Sep 20, 2005
- Expiry Date
- Sep 20, 2010
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Costol" tear duct balloon dilation duct in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 17b4c13cd7ede763f18455cbef5b8d8e and manufactured by QUEST MEDICAL INC.. The authorized representative in Taiwan is FOCUS MEDICAL 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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