Taiwan FDA registration 52cf5bf0719fb463c66f60877bd0d39c
"Wenley Asia Pacific" Delmar inspection gloves
TW: “溫利亞太”德瑪檢驗手套
Taiwan·Risk Class 1·PT. WRP BUANA MULTICOPORA·Registered Oct 18, 2005 – Oct 18, 2010CancelledRegistration details
- Analysis ID
- 52cf5bf0719fb463c66f60877bd0d39c
- Customs Code
- DHA04400098804
Company information
- Manufacturer
- PT. WRP BUANA MULTICOPORA
- Manufacturer Country
- Indonesia
- Authorized Representative
- SANSOME TRADING CO., LTD.
Product details
- Intended Use
- Patient examination gloves are disposable equipment used to prevent contamination between the patient and the examiner based on medical necessity and are placed on the examiner's hands or fingers.
- Product Type (Level 1)
- J General hospital and personal use equipment
Dates and status
- Registration Date
- Oct 18, 2005
- Expiry Date
- Oct 18, 2010
- Cancellation Date
- Oct 11, 2010
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Wenley Asia Pacific" Delmar inspection gloves in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 52cf5bf0719fb463c66f60877bd0d39c and manufactured by PT. WRP BUANA MULTICOPORA. The authorized representative in Taiwan is SANSOME TRADING CO., LTD..
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