Taiwan FDA registration 4ff0af52d2c56452ef203d95c52e723d
"STERIMED" Absorbent Pad (Non-Sterile)
TW: "傑達" 吸收墊(未滅菌)
Taiwan·Risk Class 1·MD·STERIMED S.R.O.·Registered Jul 17, 2020 – Jul 17, 2025CancelledRegistration details
- Analysis ID
- 4ff0af52d2c56452ef203d95c52e723d
- License Form
- Ministry of Health Medical Device Import No. 021752
- Customs Code
- DHA09402175201
Company information
- Manufacturer
- STERIMED S.R.O.
- Manufacturer Country
- Czechia
- Authorized Representative
- Jetstar International Corporation
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5300 Medical Absorbent Fiber
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 17, 2020
- Expiry Date
- Jul 17, 2025
- Cancellation Date
- Mar 27, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "STERIMED" Absorbent Pad (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4ff0af52d2c56452ef203d95c52e723d and manufactured by STERIMED S.R.O.. The authorized representative in Taiwan is Jetstar International Corporation.
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