Taiwan FDA registration 2b1c9783c189e8eed81287f70033d05f

"NAGASHIMA" Laryngostroboscope (Non-Sterile)

TW: "那蓋系麻" 喉頭閃頻內視鏡 (未滅菌)

Taiwan·Risk Class 1·MD·NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.·Registered Mar 03, 2014 – Mar 03, 2024Expired

Registration details

Analysis ID: 2b1c9783c189e8eed81287f70033d05f
License Form: Ministry of Health Medical Device Import No. 013903
Customs Code: DHA09401390300

Company information

Manufacturer: NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Japan
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: Mar 03, 2014
Expiry Date: Mar 03, 2024

About this record

Access comprehensive regulatory information for "NAGASHIMA" 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 2b1c9783c189e8eed81287f70033d05f and manufactured by NAGASHIMA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

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