Taiwan FDA registration 38e753156834bbd1a9ec18b0afc524a7

"Weick" manual instruments for general surgery ~ clamps, vascular recognition ring and blade (unsterilized)

TW: "偉克" 一般手術用手動式器械~夾鉗，血管識別環與刀片 (未滅菌)

Taiwan·Risk Class 1·WECK CLOSURE SYSTEMS·Registered Nov 22, 2005 – Nov 22, 2010Cancelled

Registration details

Analysis ID: 38e753156834bbd1a9ec18b0afc524a7
Customs Code: DHA04400207702

Company information

Manufacturer: WECK CLOSURE SYSTEMS
Manufacturer Country: United States
Authorized Representative: BARD PACIFIC HEALTH CARE CO., LTD.

Product details

Intended Use: General surgical hand devices are non-dynamic, hand-held or hand-operated devices that can be used repeatedly or discarded immediately after use, and are used in a variety of general procedures.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Import Information: import

Dates and status

Registration Date: Nov 22, 2005
Expiry Date: Nov 22, 2010
Cancellation Date: Jan 18, 2013

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Weick" manual instruments for general surgery ~ clamps, vascular recognition ring and blade (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38e753156834bbd1a9ec18b0afc524a7 and manufactured by WECK CLOSURE SYSTEMS. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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