"Helena" capillary electrophoresis analyzer (unsterilized)
- Analysis ID
- ec2fc620b9a1a6d619f3fe0f1d382e0d
- Customs Code
- DHA04401039509
- Manufacturer
- HELENA LABORATORIES CORP.
- Manufacturer Country
- United States
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
- Intended Use
- Limited to the first level identification scope of "Electrophoresis Equipment for Clinical Use (A.2485)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2485 Electrophoresis equipment for clinical use
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- May 25, 2011
- Expiry Date
- May 25, 2026
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Helena" capillary electrophoresis analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec2fc620b9a1a6d619f3fe0f1d382e0d and manufactured by HELENA LABORATORIES CORP.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HELENA LABORATORIES CORP., 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.