Taiwan FDA registration b2be02bec360c75c96996297a33ac669

"M. I. ONE" Laryngostroboscope (Non-Sterile)

TW: "恩艾萬" 喉頭閃頻內視鏡 (未滅菌)

Taiwan·Risk Class 1·MD·M.I.ONE CO., LTD·Registered Dec 18, 2019 – Dec 18, 2024Expired

Registration details

Analysis ID: b2be02bec360c75c96996297a33ac669
License Form: Ministry of Health Medical Device Import No. 021112
Customs Code: DHA09402111201

Company information

Manufacturer: M.I.ONE 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: Dec 18, 2019
Expiry Date: Dec 18, 2024

About this record

Access comprehensive regulatory information for "M. I. ONE" 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 b2be02bec360c75c96996297a33ac669 and manufactured by M.I.ONE CO., LTD. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

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