Taiwan FDA registration cf14638fbd4f043e443b36e26f58f430
Bioresearch Antistreptocin-O Reagent X1 (Sterilized)
TW: 生研抗鏈球菌素-O 試劑 X1 (滅菌)
Taiwan·Risk Class 1·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Jun 14, 2007 – Jun 14, 2022CancelledRegistration details
- Analysis ID
- cf14638fbd4f043e443b36e26f58f430
- Customs Code
- DHA04400594103
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limit the management method of medical devices: Streptococcus is an exoenzyme reagent (C.3720) grade 1 identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3720 鏈球菌屬胞外酶試劑
- Import Information
- import
Dates and status
- Registration Date
- Jun 14, 2007
- Expiry Date
- Jun 14, 2022
- Cancellation Date
- Jun 28, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷;;許可證已逾有效期
About this record
Access comprehensive regulatory information for Bioresearch Antistreptocin-O Reagent X1 (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cf14638fbd4f043e443b36e26f58f430 and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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