Taiwan FDA registration 77088826e4667711ceabdeff0cd16d1e

"Integra" Ear, nose, and throat manual surgical instrument (Sterile)

TW: "英特格爾" 耳鼻喉手動式外科器械 (滅菌)

Taiwan·Risk Class 1·MD·INTEGRA YORK PA, INC.·Registered Oct 18, 2016 – Oct 18, 2026Active

Registration details

Analysis ID: 77088826e4667711ceabdeff0cd16d1e
License Form: Ministry of Health Medical Device Import No. 017095
Customs Code: DHA09401709502

Company information

Manufacturer: INTEGRA YORK PA, INC.
Manufacturer Country: United States
Authorized Representative: ANGEL MEDICAL INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G4420 OTOLARYNGARY Manual Surgical Instrument
Import Information: Imported from abroad; GMP

Dates and status

Registration Date: Oct 18, 2016
Expiry Date: Oct 18, 2026

About this record

Access comprehensive regulatory information for "Integra" Ear, nose, and throat manual surgical instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77088826e4667711ceabdeff0cd16d1e and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is ANGEL MEDICAL INSTRUMENT CO., LTD..

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