“gke” Steri-Record Package Monitoring Indicators
Taiwan·Risk Class 2·MD·GKE-GMBH·Registered Jul 08, 2014 – Jul 08, 2024Expired- Analysis ID
- c66ee61cd7efdc97aa52b6de24212655
- License Form
- Ministry of Health Medical Device Import No. 026333
- Customs Code
- DHA05602633309
- Manufacturer
- GKE-GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Yida Industrial Co., Ltd
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J2800 Sterilization Process Indicator
- Import Information
- Imported from abroad
- Registration Date
- Jul 08, 2014
- Expiry Date
- Jul 08, 2024
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Access comprehensive regulatory information for “gke” Steri-Record Package Monitoring Indicators in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c66ee61cd7efdc97aa52b6de24212655 and manufactured by GKE-GMBH. The authorized representative in Taiwan is Yida Industrial Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GKE-GMBH, and 1 recent registrations in the same category. 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.