Taiwan FDA registration f3bf368a390740d5b518daf3385e2aa9
"Kjeldahl" microscopic ophthalmic scalpel (sterilized)
TW: "凱氏"顯微眼科手術刀(滅菌)
Registration details
- Analysis ID
- f3bf368a390740d5b518daf3385e2aa9
- Customs Code
- DHA04400275007
Company information
- Manufacturer
- KAI INDUSTRIES CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- SHIN SHENG PHARMACEUTICAL CO., LTD.
Product details
- Intended Use
- Manual eye surgery instruments are non-electric, hand-held devices designed to assist or perform eye surgery.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- import
Dates and status
- Registration Date
- Mar 01, 2006
- Expiry Date
- Mar 01, 2026
About this record
Access comprehensive regulatory information for "Kjeldahl" microscopic ophthalmic scalpel (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f3bf368a390740d5b518daf3385e2aa9 and manufactured by KAI INDUSTRIES CO., LTD.. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL 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