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“LMT” MR Diagnostics Incubator - Taiwan Registration 061da9fd536958d8f448e3d4a0e15abd

Access comprehensive regulatory information for “LMT” MR Diagnostics Incubator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 061da9fd536958d8f448e3d4a0e15abd and manufactured by LMT Medical Systems GmbH. The authorized representative in Taiwan is PROMED INSTRUMENT CO., 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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061da9fd536958d8f448e3d4a0e15abd
Registration Details
Taiwan FDA Registration: 061da9fd536958d8f448e3d4a0e15abd
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Device Details

“LMT” MR Diagnostics Incubator
TW: “列安”磁振掃描診斷用保育器
Risk Class 2
MD

Registration Details

061da9fd536958d8f448e3d4a0e15abd

Ministry of Health Medical Device Import No. 030876

DHA05603087600

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

J5410 Neonatal transport incubator

Imported from abroad

Dates and Status

Feb 12, 2018

Feb 12, 2023