Taiwan FDA registration 7aeb015e98ac6d5a48754b1ada276ffa

"New Sinati" scalpel blade (unsterilized)

TW: “新新那提”手術刀片 (未滅菌)

Taiwan·Risk Class 1·CINCINNATI SURGICAL COMPANY INC.·Registered Jan 06, 2009 – Jan 06, 2014Cancelled

Registration details

Analysis ID: 7aeb015e98ac6d5a48754b1ada276ffa
Customs Code: DHA04400736605

Company information

Manufacturer: CINCINNATI SURGICAL COMPANY INC.
Manufacturer Country: United Kingdom
Authorized Representative: PANPAC MEDICAL CORPORATION

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Jan 06, 2009
Expiry Date: Jan 06, 2014
Cancellation Date: Sep 26, 2016

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "New Sinati" scalpel 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 7aeb015e98ac6d5a48754b1ada276ffa and manufactured by CINCINNATI SURGICAL COMPANY INC.. The authorized representative in Taiwan is PANPAC MEDICAL CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.