Taiwan FDA registration 7d011ae956cfa9ca837139d9cc9fdba7
"Easy Record" sterilization record batch monitoring system
TW: “記錄易”滅菌紀錄批次監測系統
Taiwan·Risk Class 2·GKE-GMBH·Registered Apr 15, 2008 – Apr 15, 2028ActiveRegistration details
- Analysis ID
- 7d011ae956cfa9ca837139d9cc9fdba7
- Customs Code
- DHA00601879506
Company information
- Manufacturer
- GKE-GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Yida Industrial Co., Ltd
Product details
- 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)
- J.2800 Sterilization Process Indicator
- Import Information
- import
Dates and status
- Registration Date
- Apr 15, 2008
- Expiry Date
- Apr 15, 2028
About this record
Access comprehensive regulatory information for "Easy Record" sterilization record batch monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d011ae956cfa9ca837139d9cc9fdba7 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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