Taiwan FDA registration db3eacd38a6cdcd3dd204f9103ef5ede
"Seifoo" inspection gloves (unsterilized)
TW: “世豐”檢驗手套 (未滅菌)
Taiwan·Risk Class 1·PT. WRP BUANA MULTICOPORA·Registered Nov 12, 2007 – Nov 12, 2012CancelledRegistration details
- Analysis ID
- db3eacd38a6cdcd3dd204f9103ef5ede
- Customs Code
- DHA04400629006
Company information
- Manufacturer
- PT. WRP BUANA MULTICOPORA
- Manufacturer Country
- Indonesia
- Authorized Representative
- DE CROWN ENTERPRISES CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Gloves for Patient Examination (J.6250)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6250 病患檢查用手套
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 12, 2007
- Expiry Date
- Nov 12, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Seifoo" inspection gloves (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number db3eacd38a6cdcd3dd204f9103ef5ede and manufactured by PT. WRP BUANA MULTICOPORA. The authorized representative in Taiwan is DE CROWN ENTERPRISES CO., LTD..
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