Taiwan FDA registration 9cdab07fd0428bd8a4ea954ff4e739a7

"KURZ" Prosthesis modification instrument for ossicular replacement surgery (non-sterile)

TW: "克爾" 聽小骨置換物修正用器械 (未滅菌)

Taiwan·Risk Class 1·MD·Heinz Kurz GmbH·Registered Jun 01, 2020 – Jun 01, 2025Expired

Registration details

Analysis ID: 9cdab07fd0428bd8a4ea954ff4e739a7
License Form: Ministry of Health Medical Device Import No. 021603
Customs Code: DHA09402160307

Company information

Manufacturer: Heinz Kurz GmbH
Manufacturer Country: Germany
Authorized Representative: FU TAI TRADING CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Devices for Correction of Ossicle Replacement (G.3540)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G3540 Instrument for Hearing Bone Replacement Correction
Import Information: Imported from abroad

Dates and status

Registration Date: Jun 01, 2020
Expiry Date: Jun 01, 2025

About this record

Access comprehensive regulatory information for "KURZ" Prosthesis modification instrument for ossicular replacement surgery (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 9cdab07fd0428bd8a4ea954ff4e739a7 and manufactured by Heinz Kurz GmbH. The authorized representative in Taiwan is FU TAI TRADING CO., LTD..

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