Taiwan FDA registration e9ae44084142f2e87b43cf64724220b2
Quality control tablets of Ruimai dye
TW: 銳邁 染劑之品管片
Taiwan·Risk Class 1·REMEL INC.·Registered Jul 07, 2009 – Jul 07, 2014CancelledRegistration details
- Analysis ID
- e9ae44084142f2e87b43cf64724220b2
- Customs Code
- DHA04400788809
Company information
- Manufacturer
- REMEL INC.
- Manufacturer Country
- United States
- Authorized Representative
- Qixin Biotechnology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2660 微生物鑑別及測定器材
- Import Information
- import
Dates and status
- Registration Date
- Jul 07, 2009
- Expiry Date
- Jul 07, 2014
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Quality control tablets of Ruimai dye in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e9ae44084142f2e87b43cf64724220b2 and manufactured by REMEL INC.. The authorized representative in Taiwan is Qixin Biotechnology 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