Taiwan FDA registration 5df67230e0b147260af89484225833eb
"Record easy" sterilization records vacuum simulation test
TW: “記錄易”滅菌記錄真空模擬測試
Taiwan·Risk Class 2·GKE-GMBH·Registered Dec 10, 2007 – Dec 10, 2027ActiveRegistration details
- Analysis ID
- 5df67230e0b147260af89484225833eb
- Customs Code
- DHA00601848800
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
- Dec 10, 2007
- Expiry Date
- Dec 10, 2027
About this record
Access comprehensive regulatory information for "Record easy" sterilization records vacuum simulation test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5df67230e0b147260af89484225833eb 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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