GB 9706.2-2003 English PDF

US$914.00 · In stock
Delivery: <= 4 days. True-PDF full-copy in English will be manually translated and delivered via email.
GB 9706.2-2003: Medical electrical equipment -- Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment
Status: Obsolete

GB 9706.2: Historical versions

Standard ID	USD	BUY PDF	Lead-Days	Standard Title (Description)	Status
GB 9706.2-2003	914	Add to Cart	4 days	Medical electrical equipment -- Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment	Obsolete
GB 9706.2-1991	599	Add to Cart	4 days	Medical electrical equipment--Particular requirements for safety of haemodialysis equipment	Obsolete

Similar standards

GB/T 39381.1   YY/T 1680   YY/T 1571   GB 9706.204   GB 9706.222   GB 9706.255   

Basic data

Standard ID: GB 9706.2-2003 (GB9706.2-2003)
Description (Translated English): Medical electrical equipment-Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment
Sector / Industry: National Standard
Classification of Chinese Standard: C45
Classification of International Standard: 11.040.20
Word Count Estimation: 23,279
Date of Issue: 2003-10-09
Date of Implementation: 2004-06-01
Older Standard (superseded by this standard): GB 9706.2-1991
Adopted Standard: IEC 60601-2-16-1998, IDT
Regulation (derived from): China Announcement of Newly Approved National Standards No. 13 of 2003 (No. 61 overall)
Issuing agency(ies): General Administration of Quality Supervision, Inspection and Quarantine of the People Republic of China
Summary: This Chinese standard specifies the dedicated single use hemodialysis, hemodiafiltration and hemofiltration device (see 2. 101 define) the minimum security requirements. These devices are used for medical personnel or for use under the supervision of experts, including the operation by the patient hemodialysis, hemodiafiltration and hemofiltration settings. These requirements do not apply to in vitro dedicated piping, dialyzer, dialysate concentrate, water purification equipment, peritoneal dialysis equipment (IEC 60601-2-39: 1999).

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