Taiwan FDA registration 48eb7ccfafe4f78420aeabb06255c810
"Day Trip" Cremei artificial leather hydrophilic waterproof tripping patch (sterilized)
TW: “日絆” 可麗美人工皮親水性防水絆創貼布(滅菌)
Registration details
- Analysis ID
- 48eb7ccfafe4f78420aeabb06255c810
- Customs Code
- DHA09401923907
Company information
- Manufacturer
- NICHIBAN MEDICAL CORP.
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN NIPPON KAYAKU CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the classification and grading management measures for medical equipment "hydrophilic trauma covering materials (I.4018)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4018 親水性創傷覆蓋材
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 27, 2018
- Expiry Date
- Jun 27, 2028
About this record
Access comprehensive regulatory information for "Day Trip" Cremei artificial leather hydrophilic waterproof tripping patch (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 48eb7ccfafe4f78420aeabb06255c810 and manufactured by NICHIBAN MEDICAL CORP.. The authorized representative in Taiwan is TAIWAN NIPPON KAYAKU CO., LTD..
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