Taiwan FDA registration 11904f0406dc7208888015ff70e4b537
"Junkang" latex examination gloves (unsterilized)
TW: “雋康”乳膠檢查用手套 (未滅菌)
Registration details
- Analysis ID
- 11904f0406dc7208888015ff70e4b537
- Customs Code
- DHA04401300001
Company information
- Manufacturer
- WEAR SAFE (MALAYSIA) SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- Shenglimei Rubber 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 (J6250)".
- 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
- May 09, 2013
- Expiry Date
- May 09, 2018
- Cancellation Date
- Nov 21, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Junkang" latex examination 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 11904f0406dc7208888015ff70e4b537 and manufactured by WEAR SAFE (MALAYSIA) SDN BHD. The authorized representative in Taiwan is Shenglimei Rubber 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