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Bayer lancet (sterilization) - Taiwan Registration 0bc1934be0684488b57f26b0086558ca

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.

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.

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0bc1934be0684488b57f26b0086558ca
Registration Details
Taiwan FDA Registration: 0bc1934be0684488b57f26b0086558ca
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Device Details

Bayer lancet (sterilization)
TW: "ๆ‹œ่€ณ"ๆŽก่ก€้‡(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0bc1934be0684488b57f26b0086558ca

DHA04400641704

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Dec 26, 2007

Dec 26, 2017

Dec 14, 2017

Cancellation Information

Logged out

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