Taiwan FDA registration ccba50106501ee411dea2df8e9f6b05b

"Ji Qi" Alfi Dalip Manual Gastroenterology-Urology Surgical Instruments and Their Accessories (Unsterilized)

TW: “吉銤”艾爾菲達力普手動式胃腸科-泌尿科手術器械及其附件 (未滅菌)

Taiwan·Risk Class 1·GIMMI GMBH.·Registered Jul 30, 2008 – Jul 30, 2013Cancelled

Registration details

Analysis ID: ccba50106501ee411dea2df8e9f6b05b
Customs Code: DHA04400695009

Company information

Manufacturer: GIMMI GMBH.
Manufacturer Country: Germany
Authorized Representative: GRAND MEDICAL INSTRUMENT 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: Jul 30, 2008
Expiry Date: Jul 30, 2013
Cancellation Date: Jan 09, 2017

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Ji Qi" Alfi Dalip Manual Gastroenterology-Urology 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 ccba50106501ee411dea2df8e9f6b05b and manufactured by GIMMI GMBH.. The authorized representative in Taiwan is GRAND MEDICAL INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.