Taiwan FDA registration fefbf7252c3af0168c3930952ca3baac

"Bereoti" magnifying glass and its accessories (unsterilized)

TW: “貝瑞歐堤”放大鏡及其附件(未滅菌)

Taiwan·Risk Class 1·PERIOPTIX INC.·Registered Mar 24, 2008 – Mar 24, 2013Cancelled

Registration details

Analysis ID: fefbf7252c3af0168c3930952ca3baac
Customs Code: DHA04400659900

Company information

Manufacturer: PERIOPTIX INC.
Manufacturer Country: United States
Authorized Representative: DENSO SCIENTIFIC CO., LTD.

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: Mar 24, 2008
Expiry Date: Mar 24, 2013
Cancellation Date: Jun 03, 2015

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Bereoti" magnifying glass and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fefbf7252c3af0168c3930952ca3baac and manufactured by PERIOPTIX INC.. The authorized representative in Taiwan is DENSO SCIENTIFIC CO., LTD..

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