"Dr. Lun" Eye Surgical Perfusion Device (Sterilization) - Taiwan Registration 0d1572e86e5849d779ae385e068acce5
Access comprehensive regulatory information for "Dr. Lun" Eye Surgical Perfusion Device (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d1572e86e5849d779ae385e068acce5 and manufactured by Bausch & Lomb Incorporated. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIEFFE MEDITAL S. P. A., and 1 recent registrations in the same category. 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.
Device Details
Product Details
It is limited to the first level identification scope of ophthalmic surgical perfusion devices (M.4360) in the classification and grading management measures for medical devices.
M Ophthalmology
M.4360 Perfusion device for ophthalmic surgery
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Nov 26, 2019
Nov 26, 2024

