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"ASKLEPION" Vaginal Discharge Self-Test (Non-Sterile) - Taiwan Registration dae477e107588508836abddfd8870064

Access comprehensive regulatory information for "ASKLEPION" Vaginal Discharge Self-Test (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 dae477e107588508836abddfd8870064 and manufactured by COMMON SENSE LTD. The authorized representative in Taiwan is ASKLEPION BIOTECH CO., LTD..

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dae477e107588508836abddfd8870064
Registration Details
Taiwan FDA Registration: dae477e107588508836abddfd8870064
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Device Details

"ASKLEPION" Vaginal Discharge Self-Test (Non-Sterile)
TW: "ไบžๆ–ฏๅ…‹" ้™ฐ้“ๅˆ†ๆณŒ็‰ฉPHๅ€ผๆชข้ฉ—ๆฃ’ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

dae477e107588508836abddfd8870064

Ministry of Health Medical Device Import No. 015164

DHA09401516408

Company Information

Israel

Product Details

A Clinical chemistry and clinical toxicology

A1550 Uric pH (non-quantitative) test system

Imported from abroad

Dates and Status

Apr 28, 2015

Apr 28, 2020

Jul 15, 2022

Cancellation Information

Logged out

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