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“gke” Steri-Record Autoclave Tape - Taiwan Registration ceace07aeba12a4b06c59a58c8370fd2

Access comprehensive regulatory information for “gke” Steri-Record Autoclave Tape in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ceace07aeba12a4b06c59a58c8370fd2 and manufactured by GKE-GMBH. The authorized representative in Taiwan is Yida Industrial 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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ceace07aeba12a4b06c59a58c8370fd2
Registration Details
Taiwan FDA Registration: ceace07aeba12a4b06c59a58c8370fd2
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Device Details

“gke” Steri-Record Autoclave Tape
TW: “記錄易”滅菌記錄高壓滅菌膠帶
Risk Class 2
MD

Registration Details

ceace07aeba12a4b06c59a58c8370fd2

Ministry of Health Medical Device Import No. 026332

DHA05602633207

Company Information

Germany

Product Details

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

J General hospital and personal use equipment

J2800 Sterilization Process Indicator

Imported from abroad

Dates and Status

Jul 08, 2014

Jul 08, 2024