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“BOWA” ERGO 315R - Taiwan Registration dc4b21ea30ce1230fa9a249253f35961

Access comprehensive regulatory information for “BOWA” ERGO 315R in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc4b21ea30ce1230fa9a249253f35961 and manufactured by BOWA-ELECTRONIC GMBH & CO. KG. The authorized representative in Taiwan is SMARTECH MEDICAL 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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dc4b21ea30ce1230fa9a249253f35961
Registration Details
Taiwan FDA Registration: dc4b21ea30ce1230fa9a249253f35961
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Device Details

“BOWA” ERGO 315R
TW: “博華”亞克歐血管閉合器械
Risk Class 2
MD

Registration Details

dc4b21ea30ce1230fa9a249253f35961

Ministry of Health Medical Device Import No. 036410

DHA05603641007

Company Information

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Feb 13, 2023

Feb 13, 2028