Taiwan FDA registration e3b4beef93bb9fe614ef12104298617c
"Boehringer" Rebreathing device (Non-Sterile)
TW: "寶靈格"再吸入裝置(未滅菌)
Taiwan·Risk Class 1·MD·Boehringer Laboratories, LLC·Registered Oct 13, 2014 – Oct 13, 2019CancelledRegistration details
- Analysis ID
- e3b4beef93bb9fe614ef12104298617c
- License Form
- Ministry of Health Medical Device Import No. 014559
- Customs Code
- DHA09401455900
Company information
- Manufacturer
- Boehringer Laboratories, LLC
- Manufacturer Country
- United States
- Authorized Representative
- NSH MEDICAL CORP.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5675 Reinhalation device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 13, 2014
- Expiry Date
- Oct 13, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Boehringer" Rebreathing device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e3b4beef93bb9fe614ef12104298617c and manufactured by Boehringer Laboratories, LLC. The authorized representative in Taiwan is NSH MEDICAL CORP..
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