Taiwan FDA registration be5c8c2f7128785d60fd90cb14b69503
"Babysitter" laryngeal airway tube (sterilized)
TW: “維保姆”喉頭氣道管 (滅菌)
Taiwan·Risk Class 1·VBM MEDIZINTECHNIK GMBH·Registered Oct 30, 2007 – Oct 30, 2012CancelledRegistration details
- Analysis ID
- be5c8c2f7128785d60fd90cb14b69503
- Customs Code
- DHA04400625606
Company information
- Manufacturer
- VBM MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Giant Beam Limited
Product details
- Intended Use
- Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 30, 2007
- Expiry Date
- Oct 30, 2012
- Cancellation Date
- Aug 07, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Babysitter" laryngeal airway tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be5c8c2f7128785d60fd90cb14b69503 and manufactured by VBM MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is Giant Beam Limited.
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