"Deutschland" automatic plasma platen system
Taiwan·Risk Class 2·FRESENIUS KABI AG;; SANMINA-SCI·Registered Nov 30, 2010 – Mar 28, 2016Cancelled- Analysis ID
- 58171ba3eb2b044207151f938d83a7bb
- Customs Code
- DHA00602181802
- Manufacturer
- FRESENIUS KABI AG;; SANMINA-SCI
- Manufacturer Country
- Sweden;;Germany
- Authorized Representative
- FRESENIUS KABI TAIWAN LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.0002 Blood Component Extraction Apparatus
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Nov 30, 2010
- Expiry Date
- Mar 28, 2016
- Cancellation Date
- Aug 14, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
Top companies providing products similar to ""Deutschland" automatic plasma platen system"
Recently registered similar products
Access comprehensive regulatory information for "Deutschland" automatic plasma platen system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58171ba3eb2b044207151f938d83a7bb and manufactured by FRESENIUS KABI AG;; SANMINA-SCI. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FRESENIUS KABI AG, and 1 recent registrations in the same category. 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.