Taiwan FDA registration d41ef6828fae2b146d75862590ceb3f9
“LMB” LUXOmatic dual press system
TW: “艾爾畢”雙袋式自動血液成分壓取系統
Taiwan·Risk Class 2·MD·LMB TECHNOLOGIE GMBH·Registered Apr 24, 2018 – Apr 24, 2028ActiveRegistration details
- Analysis ID
- d41ef6828fae2b146d75862590ceb3f9
- License Form
- Ministry of Health Medical Device Import No. 030545
- Customs Code
- DHA05603054500
Company information
- Manufacturer
- LMB TECHNOLOGIE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- AMAZING MEDICAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B0002 Blood component extraction device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 24, 2018
- Expiry Date
- Apr 24, 2028
About this record
Access comprehensive regulatory information for “LMB” LUXOmatic dual press system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d41ef6828fae2b146d75862590ceb3f9 and manufactured by LMB TECHNOLOGIE GMBH. The authorized representative in Taiwan is AMAZING MEDICAL INC..
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