Taiwan FDA registration 5f82adf962066e7d2ed24fa6421dba1a

"Atrium" Vascular Tunneler (Non-Sterile)

TW: "亞翠恩"血管隧道器(未滅菌)

Taiwan·Risk Class 1·MD·Atrium Medical Corporation·Registered Dec 12, 2017 – Dec 12, 2027Active

Registration details

Analysis ID: 5f82adf962066e7d2ed24fa6421dba1a
License Form: Ministry of Health Medical Device Import No. 018600
Customs Code: DHA09401860004

Company information

Manufacturer: Atrium Medical Corporation
Manufacturer Country: United States
Authorized Representative: GETINGE GROUP TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).
Product Type (Level 1): E Cardiovascular devices
Product Type (Level 2): E4500 Cardiovascular Surgical Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Dec 12, 2017
Expiry Date: Dec 12, 2027

About this record

Access comprehensive regulatory information for "Atrium" Vascular Tunneler (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f82adf962066e7d2ed24fa6421dba1a and manufactured by Atrium Medical Corporation. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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