Taiwan FDA registration da6fa2ef450bea31a3446556ee5ef4b8

"MITSUHIRO" OTOLARYNGARY Manual Surgical Instrument (Unsterilized)

TW: "光弘" 耳鼻喉手動式外科器械 (未滅菌)

Taiwan·Risk Class 1·COHO BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Nov 13, 2019 – Nov 13, 2024Expired

Registration details

Analysis ID: da6fa2ef450bea31a3446556ee5ef4b8

Company information

Manufacturer: COHO BIOMEDICAL TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: COHO BIOMEDICAL TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the classification and grading management method for medical equipment "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4420 Otolaryngology manual surgical instruments
Import Information: Domestic

Dates and status

Registration Date: Nov 13, 2019
Expiry Date: Nov 13, 2024
Cancellation Date: Sep 19, 2024

About this record

Access comprehensive regulatory information for "MITSUHIRO" OTOLARYNGARY Manual Surgical Instrument (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number da6fa2ef450bea31a3446556ee5ef4b8 and manufactured by COHO BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is COHO BIOMEDICAL TECHNOLOGY CO., LTD..

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