Taiwan FDA registration f5af592c6ef97cc2043aaea597e09714

“Honburg” Obstetric-Gynecologic Specialized Manual Instrument (Non-Sterile)

TW: “漢博格” 婦產科專用手動器械 (未滅菌)

Taiwan·Risk Class 1·MD·HONBURG INSTRUMENTE GMBH·Registered Mar 04, 2021 – Mar 04, 2026Expired

Registration details

Analysis ID: f5af592c6ef97cc2043aaea597e09714
License Form: Ministry of Health Medical Device Import No. 022354
Customs Code: DHA09402235404

Company information

Manufacturer: HONBURG INSTRUMENTE GMBH
Manufacturer Country: Germany
Authorized Representative: HONG SHENG MEDICAL INSTRUMENTS CO.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for Obstetrics and Gynecology (L.4530)".
Product Type (Level 1): l Devices for obstetrics and gynecology
Product Type (Level 2): L4530 Manual instruments for obstetrics and gynecology
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 04, 2021
Expiry Date: Mar 04, 2026

About this record

Access comprehensive regulatory information for “Honburg” Obstetric-Gynecologic Specialized Manual Instrument (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 f5af592c6ef97cc2043aaea597e09714 and manufactured by HONBURG INSTRUMENTE GMBH. The authorized representative in Taiwan is HONG SHENG MEDICAL INSTRUMENTS CO..

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