Taiwan FDA registration f5d951d6b6cab548249d8dad7859a76b
“Sleeping Well” Oropharyngeal Airway (Non-Sterile)
TW: “利品維”口咽氣道管（未滅菌）
Taiwan·Risk Class 1·MD·SLEEPING WELL, LLC.·Registered Sep 10, 2013 – Sep 10, 2018CancelledRegistration details
- Analysis ID
- f5d951d6b6cab548249d8dad7859a76b
- License Form
- Ministry of Health Medical Device Import No. 013395
- Customs Code
- DHA09401339504
Company information
- Manufacturer
- SLEEPING WELL, LLC.
- Manufacturer Country
- United States
- Authorized Representative
- AIREX CORP.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5110 Oropharyngeal airway tube
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 10, 2013
- Expiry Date
- Sep 10, 2018
- 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 “Sleeping Well” Oropharyngeal Airway (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 f5d951d6b6cab548249d8dad7859a76b and manufactured by SLEEPING WELL, LLC.. The authorized representative in Taiwan is AIREX CORP..
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