Taiwan FDA registration 7cb05c6e56febe5c1a494172fc6f2db2
"Febim" pressurized infusion machine (unsterilized)
TW: “費比姆”加壓輸液機(未滅菌)
Taiwan·Risk Class 1·VBM MEDIZINTECHNIK GMBH·Registered Sep 16, 2009 – Sep 16, 2029ActiveRegistration details
- Analysis ID
- 7cb05c6e56febe5c1a494172fc6f2db2
- Customs Code
- DHA04400810508
Company information
- Manufacturer
- VBM MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- NSH MEDICAL CORP.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method for medical equipment "Pressure apparatus for intravenous infusion bags (J.5420)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5420 靜脈輸液袋用壓力器
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 16, 2009
- Expiry Date
- Sep 16, 2029
About this record
Access comprehensive regulatory information for "Febim" pressurized infusion machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7cb05c6e56febe5c1a494172fc6f2db2 and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is NSH MEDICAL CORP..
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