Taiwan FDA registration cde4282c17494d67801e5ced089016a6
"Gryphus" Microorganism IVD Kit (Non-sterile)
TW: "葛萊佛士" 微生物檢驗試劑套組 (未滅菌)
Registration details
- Analysis ID
- cde4282c17494d67801e5ced089016a6
- License Form
- Ministry of Health Medical Device Import No. 016721
- Customs Code
- DHA09401672106
Company information
- Manufacturer
- GRYPHUS DIAGNOSTICS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- BioChain 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 devices
- Product Type (Level 2)
- C2660 Microbial identification and assay equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 30, 2016
- Expiry Date
- Jun 30, 2021
About this record
Access comprehensive regulatory information for "Gryphus" Microorganism IVD Kit (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cde4282c17494d67801e5ced089016a6 and manufactured by GRYPHUS DIAGNOSTICS, LLC. The authorized representative in Taiwan is BioChain 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