"Sleeping Well" Oropharyngeal Airway (Non-Sterile)
Taiwan·Risk Class 1·MD·SLEEPING WELL, LLC.·Registered Mar 06, 2019 – Mar 06, 2024Expired- Analysis ID
- d9cfaac1cd80d0310c9a30ee94ca1284
- License Form
- Ministry of Health Medical Device Import No. 020142
- Customs Code
- DHA09402014205
- Manufacturer
- SLEEPING WELL, LLC.
- Manufacturer Country
- United States
- Authorized Representative
- AIREX CORP.
- 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 Devices for anesthesiology
- Product Type (Level 2)
- D5110 Oropharyngeal airway tube
- Import Information
- Imported from abroad
- Registration Date
- Mar 06, 2019
- Expiry Date
- Mar 06, 2024
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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 d9cfaac1cd80d0310c9a30ee94ca1284 and manufactured by SLEEPING WELL, LLC.. The authorized representative in Taiwan is AIREX CORP..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SLEEPING WELL, LLC., and 1 recent registrations in the same category. 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.