Taiwan FDA registration 71e7341e630a579e56d7ee4d3360ca13

"Lanke Regent" Geimei guidewire

TW: "藍克麗晶" 吉美導絲

Taiwan·MANUFACTURED FOR ANGIODYNAMICS BY: LAKE REGION MANUFATURING CO. INC.·Registered Jan 10, 2002 – Jan 10, 2007Cancelled

Registration details

Analysis ID: 71e7341e630a579e56d7ee4d3360ca13
Customs Code: DHA00600980304

Company information

Manufacturer: MANUFACTURED FOR ANGIODYNAMICS BY: LAKE REGION MANUFATURING CO. INC.
Manufacturer Country: United States
Authorized Representative: PROMEDEX CO., LTD.

Product details

Product Type (Level 1): E Cardiovascular Medicine Science
Import Information: import

Dates and status

Registration Date: Jan 10, 2002
Expiry Date: Jan 10, 2007
Cancellation Date: Nov 30, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Lanke Regent" Geimei guidewire in Taiwan's medical device market through Pure Global AI's free database. is registered under number 71e7341e630a579e56d7ee4d3360ca13 and manufactured by MANUFACTURED FOR ANGIODYNAMICS BY: LAKE REGION MANUFATURING CO. INC.. The authorized representative in Taiwan is PROMEDEX CO., LTD..

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