Taiwan FDA registration 064d29d3ed723adbfcaa3c0ca9336975

"Flexicare" Rigid Laryngoscope (Non-Sterile)

TW: "菲力斯可" 硬式喉頭鏡 (未滅菌)

Taiwan·Risk Class 1·MD·FLEXICARE MEDICAL LIMITED.·Registered Jan 12, 2017 – Jan 12, 2027Active

Registration details

Analysis ID: 064d29d3ed723adbfcaa3c0ca9336975
License Form: Ministry of Health Medical Device Import No. 017407
Customs Code: DHA09401740705

Company information

Manufacturer: FLEXICARE MEDICAL LIMITED.
Manufacturer Country: United Kingdom
Authorized Representative: HUILI MEDICAL EQUIPMENT LIMITED

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Rigid Laryngoscopy (D.5540)".
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5540 Rigid laryngoscope
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 12, 2017
Expiry Date: Jan 12, 2027

About this record

Access comprehensive regulatory information for "Flexicare" Rigid Laryngoscope (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 064d29d3ed723adbfcaa3c0ca9336975 and manufactured by FLEXICARE MEDICAL LIMITED.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.

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