Taiwan FDA registration f3bf368a390740d5b518daf3385e2aa9

"Kjeldahl" microscopic ophthalmic scalpel (sterilized)

TW: "凱氏"顯微眼科手術刀(滅菌)
Taiwan flagTaiwan·Risk Class 1·KAI INDUSTRIES CO., LTD.·Registered Mar 01, 2006 – Mar 01, 2026Expired
Registration details
Analysis ID
f3bf368a390740d5b518daf3385e2aa9
Customs Code
DHA04400275007
Company information
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