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Lemili contraceptive device - Taiwan Registration 972b4b05c3be3aa6db86cc0e917648eb

Access comprehensive regulatory information for Lemili contraceptive device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 972b4b05c3be3aa6db86cc0e917648eb and manufactured by Bayer AG; BAYER OY. The authorized representative in Taiwan is BAYER TAIWAN COMPANY LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including LEIRAS OY, OUTOKUMPU LTD, and 2 recent registrations in the same category. 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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972b4b05c3be3aa6db86cc0e917648eb
Registration Details
Taiwan FDA Registration: 972b4b05c3be3aa6db86cc0e917648eb
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Device Details

Lemili contraceptive device
TW: ๆจ‚ๆฏ้บ—้ฟๅญ•ๅ™จ
Risk Class 2
Cancelled

Registration Details

972b4b05c3be3aa6db86cc0e917648eb

DHA00600690803

Company Information

Finland;;Germany

Product Details

2699 Other devices for pregnancy avoidance

import

Dates and Status

May 10, 1993

May 10, 2023

Nov 07, 2022

Cancellation Information

Logged out

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