Taiwan FDA registration 1129eb9f589c3b073974fecca3da37dd

"Du Ke" manual ophthalmic surgery instrument (unsterile)

TW: "杜克" 手動式眼科手術器械 (未滅菌)

Taiwan·Risk Class 1·DUCKWORTH & KENT LTD·Registered Apr 14, 2006 – Apr 14, 2011Cancelled

Registration details

Analysis ID: 1129eb9f589c3b073974fecca3da37dd
Customs Code: DHA04400387101

Company information

Manufacturer: DUCKWORTH & KENT LTD
Manufacturer Country: United Kingdom
Authorized Representative: BIO-LIFE ENTERPRISE CO., LTD.

Product details

Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.4350 手動式眼科手術器械
Import Information: import

Dates and status

Registration Date: Apr 14, 2006
Expiry Date: Apr 14, 2011
Cancellation Date: Aug 01, 2011

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Du Ke" manual ophthalmic surgery instrument (unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1129eb9f589c3b073974fecca3da37dd and manufactured by DUCKWORTH & KENT LTD. The authorized representative in Taiwan is BIO-LIFE ENTERPRISE CO., LTD..

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