Taiwan FDA registration 2eecc30a1a40c6343f5edb766e593032
"RUMEX" SURGICAL INSTRUMENTS(Non-Sterile)
TW: "路梅克斯"外科器械(未滅菌)
Taiwan·Risk Class 1·MD·RUMEX INSTRUMENTS, LTD·Registered Jan 03, 2018 – Jan 03, 2023ExpiredRegistration details
- Analysis ID
- 2eecc30a1a40c6343f5edb766e593032
- License Form
- Ministry of Health Medical Device Import No. 018678
- Customs Code
- DHA09401867802
Company information
- Manufacturer
- RUMEX INSTRUMENTS, LTD
- Manufacturer Country
- Russian Federation
- Authorized Representative
- Glory Group medical Co., Ltd.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4500 Cardiovascular Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 03, 2018
- Expiry Date
- Jan 03, 2023
About this record
Access comprehensive regulatory information for "RUMEX" SURGICAL INSTRUMENTS(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 2eecc30a1a40c6343f5edb766e593032 and manufactured by RUMEX INSTRUMENTS, LTD. The authorized representative in Taiwan is Glory Group medical Co., Ltd..
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