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"Becht" Suction plus Concentrate (Non-Sterile) - Taiwan Registration 82168c352ca0befbaae7e6862cecdcef

Access comprehensive regulatory information for "Becht" Suction plus Concentrate (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 82168c352ca0befbaae7e6862cecdcef and manufactured by ALFRED BECHT GMBH. The authorized representative in Taiwan is DARLING INTERNATIONAL CORPORATION.

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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82168c352ca0befbaae7e6862cecdcef
Registration Details
Taiwan FDA Registration: 82168c352ca0befbaae7e6862cecdcef
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Device Details

"Becht" Suction plus Concentrate (Non-Sterile)
TW: "่ฒ่Œฒ็ˆพ" ้†ซ็™‚ๅ™จๆขฐ็ฎก่ทฏๆธ…ๆฝ”ๆถˆๆฏ’ๆถฒ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

82168c352ca0befbaae7e6862cecdcef

Ministry of Health Medical Device Import No. 018114

DHA09401811408

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".

J General hospital and personal use equipment

J6890 Disinfectants for general medical devices

Imported from abroad

Dates and Status

Jul 27, 2017

Jul 27, 2027