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"Glaxo" pandelin aspiration aid (unsterilized) - Taiwan Registration dfdf060f87232741ae4472ae7df4f60a

Access comprehensive regulatory information for "Glaxo" pandelin aspiration aid (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfdf060f87232741ae4472ae7df4f60a and manufactured by SMITHKLINE BEECHAM LIMITED. The authorized representative in Taiwan is GLAXOSMITHKLINE FAR EAST B.V., TAIWAN BRANCH (NETHERLANDS).

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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dfdf060f87232741ae4472ae7df4f60a
Registration Details
Taiwan FDA Registration: dfdf060f87232741ae4472ae7df4f60a
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Device Details

"Glaxo" pandelin aspiration aid (unsterilized)
TW: โ€œ่‘›่˜ญ็ด โ€ๆณ›ๅพ—ๆž—ๅธ่—ฅ่ผ”ๅŠฉๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dfdf060f87232741ae4472ae7df4f60a

DHA04401237309

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".

D Anesthesiology

D.5640 ้žๅ‘ผๅธ็”จ้†ซ่—ฅๅ™ด้œงๅ™จ(atomizer)

import

Dates and Status

Nov 15, 2012

Nov 15, 2017

Mar 06, 2017

Cancellation Information

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