Taiwan FDA registration f36d31f1140014c600428a4544dab5bc

"Kindy" manual gastroenterological-urological surgical instruments and their accessories (unsterilized)

TW: "金蒂"手動式胃腸科-泌尿科手術器械及其附件(未滅菌)

Taiwan·Risk Class 1·TIDI PRODUCTS, LLC·Registered May 25, 2012 – May 25, 2022Cancelled

Registration details

Analysis ID: f36d31f1140014c600428a4544dab5bc
Customs Code: DHA04401174502

Company information

Manufacturer: TIDI PRODUCTS, LLC
Manufacturer Country: United States
Authorized Representative: KING DAY CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (H.4730)".
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.4730 H.4730 Hand Gastroentero-Urology Surgical Instruments and Accessories
Import Information: import

Dates and status

Registration Date: May 25, 2012
Expiry Date: May 25, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Kindy" manual gastroenterological-urological surgical instruments and their accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f36d31f1140014c600428a4544dab5bc and manufactured by TIDI PRODUCTS, LLC. The authorized representative in Taiwan is KING DAY CO., LTD..

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