Centrifuge
Vietnam·Risk Class TBYT Loại B·UNIVERSAL 320 R·Andreas Hettich GmbH & Co.KG·Registered Oct 13, 2024- Analysis ID
- 240000071/PCBB-BN
- Submission ID
- 000.00.16.H05-241001-0005
- Product Type
- UNIVERSAL 320 R
- Manufacturer
- Andreas Hettich GmbH & Co.KG
- Product Owner
- Andreas Hettich GmbH & Co.KG
- Authorized Representative
- CÔNG TY CỔ PHẦN MEDCOMTECH
- Intended Use
- The Universal 320 R Centrifuge is a medical diagnostic in vitro device that complies with the In Vitro Diagnostic Medical Device Regulation (EU) 2017/746. The device is used to perform the centrifugation step as well as to enrich the human sample material for the subsequent diagnostic steps. The user can set up each variable physical parameter within the limits set by the device. The centrifuge is intended for use only by qualified personnel in laboratories. The centrifuge is designed for the purpose mentioned above. Correct use includes compliance with all instructions in the manual and performing the required maintenance. Any other use or use outside the scope of this purpose is considered incorrect. Andreas Hettich GmbH & Co. KG will not be liable for any damage resulting from incorrect use.
- Registration Date
- Oct 13, 2024
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Access comprehensive regulatory information for Centrifuge in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TBYT Loại B medical device is registered under number 240000071/PCBB-BN and manufactured by Andreas Hettich GmbH & Co.KG. The authorized representative in Vietnam is CÔNG TY CỔ PHẦN MEDCOMTECH.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including HERMLE LABORTECHNIK GMBH, SIGMA LABORZENTRIFUGEN GMBH, and 5 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.