Taiwan FDA registration 1926bc6c79baed852d97d097cdc2f6f5

"Jeisys" Obstetric-gynecologic general manual instrument (Non-sterile)

TW: "婕曦" 婦產科用一般手動器械 (未滅菌)

Taiwan·Risk Class 1·MD·Jeisys Medical Inc.·Registered Jan 17, 2019 – Jan 17, 2024Expired

Registration details

Analysis ID: 1926bc6c79baed852d97d097cdc2f6f5
License Form: Ministry of Health Medical Device Import No. 020034
Customs Code: DHA09402003402

Company information

Manufacturer: Jeisys Medical Inc.
Manufacturer Country: Korea, Republic of
Authorized Representative: YUNGLIN BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "General Manual Instruments for Obstetrics and Gynecology (L.4520)".
Product Type (Level 1): l Devices for obstetrics and gynecology
Product Type (Level 2): L4520 General manual instruments for obstetrics and gynecology
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 17, 2019
Expiry Date: Jan 17, 2024

About this record

Access comprehensive regulatory information for "Jeisys" Obstetric-gynecologic general 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 1926bc6c79baed852d97d097cdc2f6f5 and manufactured by Jeisys Medical Inc.. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..

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