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“Geister” CleanLoop Sterilization Container - Taiwan Registration c23ef2c1334567ac230a57802a58ceed

Access comprehensive regulatory information for “Geister” CleanLoop Sterilization Container in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c23ef2c1334567ac230a57802a58ceed and manufactured by GEISTER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is PLOVER MEDICAL INSTRUMENTS, INC..

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c23ef2c1334567ac230a57802a58ceed
Registration Details
Taiwan FDA Registration: c23ef2c1334567ac230a57802a58ceed
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Device Details

“Geister” CleanLoop Sterilization Container
TW: “杰士特”科林樂普滅菌盒
Risk Class 2
MD

Registration Details

c23ef2c1334567ac230a57802a58ceed

Ministry of Health Medical Device Import No. 031899

DHA05603189901

Company Information

Germany

Product Details

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

J General hospital and personal use equipment

J6850 sterilization kit

Imported from abroad

Dates and Status

Dec 05, 2018

Dec 05, 2023