Plasma Exchange Kit - Vietnam Registration 2400923ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Plasma Exchange Kit in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại C medical device is registered under number 2400923ĐKLH/BYT-HTTB and manufactured by Fenwal International, Inc.. The authorized representative in Vietnam is CÔNG TY CỔ PHẦN FRESENIUS KABI VIỆT NAM.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Terumo BCT Inc., Fresenius HemoCare Netherlands B.V., 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.

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2400923ĐKLH/BYT-HTTB

Registration Details

Vietnam MOH Registration: 2400923ĐKLH/BYT-HTTB

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Device Details

Plasma Exchange Kit

VN: Bộ dụng cụ trao đổi huyết tương

Risk Class TTBYT Loại C

Registration Details

Analysis ID

2400923ĐKLH/BYT-HTTB

Submission ID

000.00.04.G18-231103-0035

Product Type

PL1 Plasma Exchange Set

Product Code

9400401

Technical Details

Intended Use

The kit is used in combination with the COM.TEC automated blood component separation machine for blood plasma substitution therapy using a dual metal system, which can switch to a single metal system in emergencies. Dual metal system for red blood cell substitution/elimination.