Taiwan FDA registration ceace07aeba12a4b06c59a58c8370fd2
“gke” Steri-Record Autoclave Tape
TW: “記錄易”滅菌記錄高壓滅菌膠帶
Taiwan·Risk Class 2·MD·GKE-GMBH·Registered Jul 08, 2014 – Jul 08, 2024ExpiredRegistration details
- Analysis ID
- ceace07aeba12a4b06c59a58c8370fd2
- License Form
- Ministry of Health Medical Device Import No. 026332
- Customs Code
- DHA05602633207
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)
- J2800 Sterilization Process Indicator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 08, 2014
- Expiry Date
- Jul 08, 2024
About this record
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.
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