Taiwan FDA registration 0bc1934be0684488b57f26b0086558ca

Bayer lancet (sterilization)

TW: "拜耳"採血針(滅菌)

Taiwan·Risk Class 1·MANUFACTURED BY HTL-STREFA S.A. FOR BAYER HEALTHCARE LLC DIABETES CARE DIVISION·Registered Dec 26, 2007 – Dec 26, 2017Cancelled

Registration details

Analysis ID: 0bc1934be0684488b57f26b0086558ca
Customs Code: DHA04400641704

Company information

Manufacturer: MANUFACTURED BY HTL-STREFA S.A. FOR BAYER HEALTHCARE LLC DIABETES CARE DIVISION
Manufacturer Country: Poland
Authorized Representative: Taiwan Bayer 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: Dec 26, 2007
Expiry Date: Dec 26, 2017
Cancellation Date: Dec 14, 2017

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for Bayer lancet (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0bc1934be0684488b57f26b0086558ca and manufactured by MANUFACTURED BY HTL-STREFA S.A. FOR BAYER HEALTHCARE LLC DIABETES CARE DIVISION. The authorized representative in Taiwan is Taiwan Bayer Co., Ltd.

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