“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.
Device Details
Registration Details
ceace07aeba12a4b06c59a58c8370fd2
Ministry of Health Medical Device Import No. 026332
DHA05602633207
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

