Taiwan FDA registration 6f969d10de860d925dc59c8bd7991aa2

"MEDIANA" Laryngostroboscope (Non-Sterile)

TW: "美帝那" 喉頭閃頻內視鏡 (未滅菌)

Taiwan·Risk Class 1·MD·MEDIANA CO., LTD.·Registered May 28, 2019 – May 28, 2024Expired

Registration details

Analysis ID: 6f969d10de860d925dc59c8bd7991aa2
License Form: Ministry of Health Medical Device Import No. 020494
Customs Code: DHA09402049400

Company information

Manufacturer: MEDIANA CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: WHOLE WELL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Laryngeal Flash Endoscopy (G.4750)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G4750 Laryngeal flash endoscope
Import Information: Imported from abroad

Dates and status

Registration Date: May 28, 2019
Expiry Date: May 28, 2024

About this record

Access comprehensive regulatory information for "MEDIANA" Laryngostroboscope (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 6f969d10de860d925dc59c8bd7991aa2 and manufactured by MEDIANA CO., LTD.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

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