Taiwan FDA registration 8fe42c6548fe8298738533aa94a994dd

"Sleeping well" Oropharyngeal airway (Non-Sterile)

TW: "詩利品" 口咽氣道管 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SLEEPING WELL, LLC.·Registered Jun 04, 2014 – Jun 04, 2019Cancelled
Registration details
Analysis ID
8fe42c6548fe8298738533aa94a994dd
License Form
Ministry of Health Medical Device Import No. 014209
Customs Code
DHA09401420902
Company information
Manufacturer Country
United States
Authorized Representative
Den Mate 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
Jun 04, 2014
Expiry Date
Jun 04, 2019
Cancellation Date
Jun 07, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 8fe42c6548fe8298738533aa94a994dd and manufactured by SLEEPING WELL, LLC.. The authorized representative in Taiwan is Den Mate 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.

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