GB12260-2017

Cardiopulmonary bypass systems—Roller blood pump

心肺转流系统滚压式血泵

GB 12260-2017 ist eine gültige verbindliche chinesische Nationalnorm: Cardiopulmonary bypass systems—Roller blood pump. Branchencluster: Lebensmittel. Schwerpunkt: Produktsicherheit. Inkrafttreten: 1. Juli 2019.

Die Anwendbarkeit hängt vom Produktumfang, dem Zertifizierungsweg, Bekanntmachungen der Behörden und Übergangsregeln ab. Fordern Sie eine Übersetzung an oder prüfen Sie die Quelle, bevor Sie diesen Eintrag für Compliance-Entscheidungen nutzen.

Compliance-Überblick

Dieser Überblick ist derzeit nur auf Englisch verfügbar.

Geltungsbereich und Anwendbarkeit

This standard applies to cardiopulmonary bypass systems specifically utilizing roller blood pumps. It is designed for medical facilities performing surgeries or emergency rescues where the pump temporarily replaces heart function for extracorporeal circulation or local perfusion. Compliance with this standard is mandatory for all manufacturers of these specific medical devices. It does not apply to other types of blood pumps or cardiopulmonary bypass equipment outside the roller pump category.

Technische Anforderungen

The standard outlines comprehensive performance and safety parameters for roller blood pumps. It specifies requirements for both constant flow and pulsatile flow operations, including flow rate tolerances, maximum flow capacities, and rotational speed accuracy. Manufacturers must ensure that their pumps meet the strict performance metrics for both operational modes. Mechanical integrity is heavily emphasized, with specific requirements for roller radial runout, synchronization errors between rollers, and coaxiality between the central axis and the pump body. The standard also mandates specific safety monitoring functions, including pressure, temperature, and time monitoring, as well as critical bubble detection and blood level detection capabilities to automatically halt operation during adverse events. Environmental adaptability and electrical safety are also covered. The equipment must withstand specific climate and mechanical environmental tests as referenced in GB/T 14710-2009, and must comply with the general safety requirements for medical electrical equipment outlined in GB 9706.1 and GB 9706.15. Proper noise level limitations and structural integrity under normal working conditions are also strictly enforced.

Prüfverfahren

Testing procedures involve visual inspections for structural integrity and utilizing precision instruments like dial indicators to measure mechanical tolerances such as roller runout and synchronization errors. Flow and speed accuracy are tested using water as a blood substitute under specific pressure conditions. Safety features are evaluated by simulating critical conditions, such as injecting specific volumes of air for bubble detection or manipulating blood levels for automatic pump halt testing. Noise levels are measured using an A-weighted sound level meter at a specified distance from the pump head.

Häufige Fragen

What products are regulated under GB 12260-2017?

GB 12260-2017 specifically regulates cardiopulmonary bypass systems that utilize roller blood pumps used for extracorporeal circulation or local perfusion during surgeries.

Is GB 12260-2017 a mandatory standard?

Yes, all technical content within GB 12260-2017 is mandatory for manufacturers producing roller blood pumps for the Chinese market.

What are the key safety monitoring requirements in this standard?

The standard requires pumps to have pressure monitoring, temperature monitoring, at least three timers, bubble detection (for bubbles >0.065mL), and blood level monitoring with automatic pump stop functions.

The summary above provides a high-level overview of GB 12260-2017. To ensure complete compliance for your products entering the Chinese market, a precise and professional translation of the full technical specifications is essential. Purchase our high-quality English translation of GB 12260-2017 today to access all detailed parameters, tables, and testing procedures.

Hinweise zur Anwendbarkeit

Normtyp: Produkt
CCS: C45
ICS: 11.040.40
Zuständige Behörde: National Medical Products Administration
Technisches Komitee: National Technical Committee on Medical Extracorporeal Circulation Equipment of Standardization Administration of China

Normbeziehungen

Ersetzt:GB 12260-2005