Taiwan FDA registration 3c5914473f9c58df5045dccbee218466

"Mitoyo" electric body fluid aspirator (unsterilized)

TW: "三豐" 電動體液吸引器 (未滅菌)

Taiwan·Risk Class 1·Mitutoyo Medical Equipment Co., Ltd·Registered Dec 29, 2005 – Dec 29, 2010Cancelled

Registration details

Analysis ID: 3c5914473f9c58df5045dccbee218466
Customs Code: DHY04300087105

Company information

Manufacturer: Mitutoyo Medical Equipment Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Mitutoyo Medical Equipment Co., Ltd

Product details

Intended Use: Apparatus used to suction, remove, or sample bodily fluids. Powered by an external vacuum source. The equipment includes a vacuum regulator, a vacuum collection bottle, a suction catheter and end, a fitting of an elastic suction tube, a hard suction end, a sampling snare, a non-injurious tube and a suction regulator (scaled)
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: Domestic

Dates and status

Registration Date: Dec 29, 2005
Expiry Date: Dec 29, 2010
Cancellation Date: Nov 23, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Mitoyo" electric body fluid aspirator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3c5914473f9c58df5045dccbee218466 and manufactured by Mitutoyo Medical Equipment Co., Ltd. The authorized representative in Taiwan is Mitutoyo Medical Equipment Co., Ltd.

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