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“Keeler” Slit Lamp and accessories - Taiwan Registration 51317b8e292a8677ff06b0a8fd52b89f

Access comprehensive regulatory information for “Keeler” Slit Lamp and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51317b8e292a8677ff06b0a8fd52b89f and manufactured by KEELER LTD.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT 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.

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51317b8e292a8677ff06b0a8fd52b89f
Registration Details
Taiwan FDA Registration: 51317b8e292a8677ff06b0a8fd52b89f
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Device Details

“Keeler” Slit Lamp and accessories
TW: “奇勒”裂隙燈及其附件
Risk Class 2
MD

Registration Details

51317b8e292a8677ff06b0a8fd52b89f

Ministry of Health Medical Device Import No. 032319

DHA05603231901

Company Information

United Kingdom

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M1850 AC power type fine gap lamp

Imported from abroad

Dates and Status

Mar 28, 2019

Mar 28, 2024