Taiwan FDA registration 6bdf8b6feee8da68237b7542dc83f442
"Bayer" urine glucose test lozenges
TW: "拜耳"尿葡萄糖試驗錠
Registration details
- Analysis ID
- 6bdf8b6feee8da68237b7542dc83f442
- Customs Code
- DHA00601487602
Company information
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Taiwan Bayer Co., Ltd
Product details
- Intended Use
- Semi-quantitative measurement of glucose in urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1340 Urine glucose (non-quantitative) test system
- Import Information
- import
Dates and status
- Registration Date
- Nov 21, 2005
- Expiry Date
- Nov 21, 2010
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bayer" urine glucose test lozenges in Taiwan's medical device market through Pure Global AI's free database. is registered under number 6bdf8b6feee8da68237b7542dc83f442 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