Taiwan FDA registration b7bc4c1deaa8f9171504f81c0d98cb22
"Bayer" urine test strip - urine ketone test strip
TW: "拜耳"尿液試驗試紙-尿酮體試驗試紙
Taiwan·Risk Class 1·BAYER DIAGNOSTICS MANUFACTURING LIMITED - BRIDGEND SITE·Registered May 24, 2007 – May 24, 2012CancelledRegistration details
- Analysis ID
- b7bc4c1deaa8f9171504f81c0d98cb22
- Customs Code
- DHA04400590206
Company information
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Taiwan Bayer Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the "Ketone (Non-quantitative) Test System (A.1435)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1435 Ketone (non-quantitative) testing system
- Import Information
- import
Dates and status
- Registration Date
- May 24, 2007
- Expiry Date
- May 24, 2012
- Cancellation Date
- Apr 03, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bayer" urine test strip - urine ketone test strip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b7bc4c1deaa8f9171504f81c0d98cb22 and manufactured by BAYER DIAGNOSTICS MANUFACTURING LIMITED - BRIDGEND SITE. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices