Taiwan FDA registration 0d3f743525c8dd03897a68247f6bfc6f

"Nidris" Topical Rinse Sleeve (Sterilized)

TW: "尼得立斯" 外用沖洗套 (滅菌)

Taiwan·Risk Class 1·Jiacheng Seiko Co., Ltd. second factory·Registered Jan 30, 2016 – Jan 30, 2021Cancelled

Registration details

Analysis ID: 0d3f743525c8dd03897a68247f6bfc6f

Company information

Manufacturer: Jiacheng Seiko Co., Ltd. second factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: NEEDLELESS CORPORATION

Product details

Intended Use: Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4200 Incoming/Drainage Tubes and Accessories
Import Information: 委託製造;; 國產;; QMS/QSD

Dates and status

Registration Date: Jan 30, 2016
Expiry Date: Jan 30, 2021
Cancellation Date: Sep 23, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Nidris" Topical Rinse Sleeve (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d3f743525c8dd03897a68247f6bfc6f and manufactured by Jiacheng Seiko Co., Ltd. second factory. The authorized representative in Taiwan is NEEDLELESS CORPORATION.

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