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“ERBE” BiClamp knife 220 Vessel sealing instrument - Taiwan Registration cc753b742063e5486026a83d40b44b0a

Access comprehensive regulatory information for “ERBE” BiClamp knife 220 Vessel sealing instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc753b742063e5486026a83d40b44b0a and manufactured by ERBE ELEKTROMEDIZIN GMBH. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE 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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cc753b742063e5486026a83d40b44b0a
Registration Details
Taiwan FDA Registration: cc753b742063e5486026a83d40b44b0a
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Device Details

“ERBE” BiClamp knife 220 Vessel sealing instrument
TW: “愛爾博”拋棄式百克鉗
Risk Class 2
MD

Registration Details

cc753b742063e5486026a83d40b44b0a

Ministry of Health Medical Device Import No. 036106

DHA05603610604

Company Information

Germany

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

Nov 24, 2022

Nov 24, 2027