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“Keeler” Otoscopes (Non-Sterile) - Taiwan Registration b1a82f606b120d2ca285849d5b0c05d4

Access comprehensive regulatory information for “Keeler” Otoscopes (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1a82f606b120d2ca285849d5b0c05d4 and manufactured by Keeler Limited. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..

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b1a82f606b120d2ca285849d5b0c05d4
Registration Details
Taiwan FDA Registration: b1a82f606b120d2ca285849d5b0c05d4
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Device Details

“Keeler” Otoscopes (Non-Sterile)
TW: “奇勒” 耳鏡(未滅菌)
Risk Class 1
MD

Registration Details

b1a82f606b120d2ca285849d5b0c05d4

Ministry of Health Medical Device Import No. 022772

DHA09402277209

Company Information

United Kingdom

Product Details

Limited to the first level identification range of the "Otoscope (G.4770)" of the Administrative Measures for the Classification and Grading of Medical Equipment.

G ENT Science

G4770 Otoscope

Imported from abroad

Dates and Status

Mar 29, 2022

Mar 29, 2027