Taiwan FDA registration be6520fa2e95287b426e1c48239ed1b3

"Tuoren" Video Intubation Stylet (Non-Sterile)

TW: "駝人" 影像式氣管內管探針 (未滅菌)

Taiwan·Risk Class 1·MD·TUOREN MEDICAL DEVICE INDIA PVT LTD·Registered Dec 12, 2018 – Dec 12, 2023Expired

Registration details

Analysis ID: be6520fa2e95287b426e1c48239ed1b3
License Form: Ministry of Health Medical Device Import No. 019908
Customs Code: DHA09401990801

Company information

Manufacturer: TUOREN MEDICAL DEVICE INDIA PVT LTD
Manufacturer Country: India
Authorized Representative: BIOTRONIC INSTRUMENT ENTERPRISE LTD.

Product details

Intended Use: Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5790 Endotracheal Probe
Import Information: Imported from abroad

Dates and status

Registration Date: Dec 12, 2018
Expiry Date: Dec 12, 2023

About this record

Access comprehensive regulatory information for "Tuoren" Video Intubation Stylet (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 be6520fa2e95287b426e1c48239ed1b3 and manufactured by TUOREN MEDICAL DEVICE INDIA PVT LTD. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..

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