Taiwan FDA registration 792ad9b7819536c3ea940ad815bd3469
“Raumedic” Neuromonitoring system
TW: “諾美德科”顱內監測器
Registration details
- Analysis ID
- 792ad9b7819536c3ea940ad815bd3469
- License Form
- Ministry of Health Medical Device Import No. 030845
- Customs Code
- DHA05603084502
Company information
- Manufacturer
- RAUMEDIC AG
- Manufacturer Country
- Germany
- Authorized Representative
- SYNERGY BIOMEDICAL LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K1620 Intracranial Pressure Monitor Material
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 31, 2018
- Expiry Date
- Jan 31, 2028
About this record
Access comprehensive regulatory information for “Raumedic” Neuromonitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 792ad9b7819536c3ea940ad815bd3469 and manufactured by RAUMEDIC AG. The authorized representative in Taiwan is SYNERGY BIOMEDICAL 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