Taiwan FDA registration f3550b09caa3ef797992277053779551

"Wound card" intraoperative fluorescein angiography system

TW: “倈卡” 術中螢光血管攝影系統
Taiwan flagTaiwan·Risk Class 2·LEICA MICROSYSTEMS(SCHWEIZ) AG;; LEICA INSTRUMENTS (SINGAPORE) PTE. LTD.·Registered Jan 20, 2024 – Jan 20, 2029Active
Registration details
Analysis ID
f3550b09caa3ef797992277053779551
Customs Code
DHA05603691001
Company information
Manufacturer Country
Switzerland;;Singapore
Authorized Representative
CHIU HO MEDICAL SYSTEM CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1600 X光血管攝影系統
Import Information
import
Dates and status
Registration Date
Jan 20, 2024
Expiry Date
Jan 20, 2029
About this record

Access comprehensive regulatory information for "Wound card" intraoperative fluorescein angiography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3550b09caa3ef797992277053779551 and manufactured by LEICA MICROSYSTEMS(SCHWEIZ) AG;; LEICA INSTRUMENTS (SINGAPORE) PTE. LTD.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM 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