Taiwan FDA registration a2dea0931ce0013bcd8617aeb74b1530
"Umiplus" micro skin gauze pad (sterilized)
TW: “優美加”微植皮紗布墊 (滅菌)
Registration details
- Analysis ID
- a2dea0931ce0013bcd8617aeb74b1530
- Customs Code
- DHA04400611106
Company information
- Manufacturer
- HUMECA B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- Yangzhi Biotechnology Co., Ltd
Product details
- Intended Use
- Limited to the first level of identification scope of "external use of non-absorbent gauze or sponge balls (I.4014)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4014 Non-absorbent cloth or sea balls are used externally
- Import Information
- import
Dates and status
- Registration Date
- Aug 28, 2007
- Expiry Date
- Aug 28, 2017
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Umiplus" micro skin gauze pad (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a2dea0931ce0013bcd8617aeb74b1530 and manufactured by HUMECA B.V.. The authorized representative in Taiwan is Yangzhi Biotechnology 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.
Free DatabasePowered by Pure Global AI89,000+ Devices