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"Baoer" ovulation test reagent (unsterilized) - Taiwan Registration 4cd626759d03eee3c53757ae23be76e1

Access comprehensive regulatory information for "Baoer" ovulation test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4cd626759d03eee3c53757ae23be76e1 and manufactured by IND DIAGNOSTIC INC.. The authorized representative in Taiwan is ELAN ACCESSORIES COMPANY 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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4cd626759d03eee3c53757ae23be76e1
Registration Details
Taiwan FDA Registration: 4cd626759d03eee3c53757ae23be76e1
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Device Details

"Baoer" ovulation test reagent (unsterilized)
TW: "ๅฏถๅ…’"ๆŽ’ๅตๆธฌ่ฉฆ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4cd626759d03eee3c53757ae23be76e1

DHA04401175607

Company Information

Canada

Product Details

Limited to the first level identification range of the "luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Equipment.

A Clinical chemistry and clinical toxicology

A.1485 Progesterone testing system

import

Dates and Status

May 28, 2012

May 28, 2017

Dec 20, 2019

Cancellation Information

Logged out

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