Taiwan FDA registration 0a88814e65e930a05a970ee8e072ffbf
"Vibime" gas pressure corrector (unsterilized)
TW: “維比姆” 氣體壓力校正器(未滅菌)
Taiwan·Risk Class 1·VBM MEDIZINTECHNIK GMBH·Registered Dec 13, 2011 – Dec 13, 2016CancelledRegistration details
- Analysis ID
- 0a88814e65e930a05a970ee8e072ffbf
- Customs Code
- DHA04401117309
Company information
- Manufacturer
- VBM MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- GRANDMEDICAL ENTERPRISE LTD.
Product details
- Intended Use
- It is limited to the scope of Class 1 identification of the "Gas Pressure Corrector (D.2620)" of the Medical Device Management Regulations.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.2620 氣體壓力校正器
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 13, 2011
- Expiry Date
- Dec 13, 2016
- Cancellation Date
- Jan 06, 2017
Cancellation information
- Status
- Logged out
- Reason
- 非屬醫療器材
About this record
Access comprehensive regulatory information for "Vibime" gas pressure corrector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0a88814e65e930a05a970ee8e072ffbf and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is GRANDMEDICAL ENTERPRISE LTD..
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