Taiwan FDA registration 04c34b6ddfb27f40d3d7b1a1360a2be6

"Geni Baby" Feeder (Unsterilized)

TW: “吉尼寶貝”餵藥器 (未滅菌)

Taiwan·Risk Class 1·The second plant of Ringe Co., Ltd·Registered Oct 28, 2008 – Oct 28, 2018Cancelled

Registration details

Analysis ID: 04c34b6ddfb27f40d3d7b1a1360a2be6

Company information

Manufacturer: The second plant of Ringe Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: JINI BABY INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Liquid Drug Dispenser (J.6430)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6430 液體藥物給藥器
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Oct 28, 2008
Expiry Date: Oct 28, 2018
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Geni Baby" Feeder (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 04c34b6ddfb27f40d3d7b1a1360a2be6 and manufactured by The second plant of Ringe Co., Ltd. The authorized representative in Taiwan is JINI BABY INTERNATIONAL 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.