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"Dr. Lun" Eye Surgical Perfusion Device (Sterilization) - Taiwan Registration 360698f6903275ede920ce849d3c456f

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 360698f6903275ede920ce849d3c456f and manufactured by BIEFFE MEDITAL S. P. A.. 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 Bausch & Lomb Incorporated, 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.

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360698f6903275ede920ce849d3c456f
Registration Details
Taiwan FDA Registration: 360698f6903275ede920ce849d3c456f
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Device Details

"Dr. Lun" Eye Surgical Perfusion Device (Sterilization)
TW: "ๅšๅฃซๅ€ซ" ็œผ็›ๆ‰‹่ก“็Œๆณจ่ฃ็ฝฎ (ๆป…่Œ)
Risk Class 1

Registration Details

360698f6903275ede920ce849d3c456f

DHA09401933006

Company Information

Italy

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

Jul 19, 2018

Jul 19, 2028

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