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Implants for surgery. Minimum data sets for surgical implants
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Basic data
| Standard ID | YY/T 0682-2008 (YY/T0682-2008) |
| Description (Translated English) | Implants for surgery. Minimum data sets for surgical implants |
| Sector / Industry | Medical Device & Pharmaceutical Industry Standard (Recommended) |
| Classification of Chinese Standard | C35 |
| Classification of International Standard | 11.040.40 |
| Word Count Estimation | 7,779 |
| Date of Issue | 2008-10-17 |
| Date of Implementation | 2010-01-01 |
| Quoted Standard | GB/T 19000-2000; YY/T 0287 |
| Adopted Standard | ISO 16054-2000, IDT |
| Regulation (derived from) | SFDA [2008] No. 605 |
| Issuing agency(ies) | State Food and Drug Administration |
| Summary | This standard specifies the order to implant registration, tracking and analysis for the purpose of removing surgical implants with a minimum data base, and its role is to facilitate the recording and international exchange of information. Group minimum data collection requirements to the implant for the purpose of tracking, so that when the device defect unexpected event occurs, the patient can track the defective device and recall. Group also meets the minimum information for the purpose to remove the analysis and research-extension data base for the purpose of cross-reference between the core data requirements. This standard applies to implantable medical devices (implants over 30d) manufacturers and distributors, as well as perform implant operations hospitals and other medical institutions. This standard specifies the specific requirements of data items, these items should be implantable medical device manufacturers and distributors, hospitals and other medical institutions at any time after implantation and when removing documented. |
YY/T 0682-2008: Implants for surgery. Minimum data sets for surgical implants
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Implants for surgery.Minimum data sets for surgical implants
ICS 11.040.40
C35
People's Republic of China pharmaceutical industry standards
YY/T 0682-2008/ISO 16054.2000
Surgical implants Surgical implants with minimal data group
(ISO 16054.2000, IDT)
Posted 2008-10-17
2010-01-01 implementation
State Food and Drug Administration issued
Foreword
This standard is identical with ISO 16054.2000 "Surgical implants Surgical implants with minimal information group."
Appendix A of this standard is an informative annex.
This standard by the national surgical implants and orthopedic instruments Standardization Technical Committee (SAC/TC110) and focal points.
This standard was drafted. Tianjin, the State Food and Drug Administration Medical Device Quality Supervision and Inspection Center.
The main drafters of this standard. Li Libin, Sun Huili, PROCEEDINGS, Furui Zhi.
YY/T 0682-2008/ISO 16054.2000
Surgical implants Surgical implants with minimal data group
1 Scope
This standard defines an implant registration, tracking and analysis for the purpose of removing the surgical implant with minimal data group, whose role is to facilitate record
And recording data on international exchange. The minimum data collection requirements to the group for the purpose of tracking implant, so that when something unexpected equipment defects
When members occurs, the patient can track and recall defective devices. Groups also meet the minimum information to take out for the purpose of analysis and research -
Mutual core information requirements for reference purposes between extended data base.
This standard applies to implantable medical devices (implants than 30d) manufacturers and distributors, as well as to perform the implantation procedure and its hospitals
His medical institutions. This standard specifies the requirements for specific information on the project, these data items by manufacturers and distributors of implantable medical devices
Providers, hospitals and other medical institutions to be recorded when the implant removed and after any time.
This standard is intended to define to record all events inserted and removed a minimum data base, while also providing quick inquiry with a specific patient groups
The implant associated data in order to track the patient, the particular patient population refers to specific patients receiving implantable device or a group of devices
overall.
This standard is not to collect information for the purpose of specific medical practitioners, the medical institutions or the manufacturer, but rather to track patients for the purpose.
Note. Users of this standard should ensure compliance with the data storage process involving national standards or laws and regulations.
2 Normative references
The following documents contain provisions which, through reference in this standard and become the standard terms. For dated references, subsequent
Amendments (not including errata content) or revisions do not apply to this standard, however, encourage the parties to the agreement are based on research
Whether the latest versions of these documents. For undated reference documents, the latest versions apply to this standard.
GB/T 19000-2000 Quality Management System - Fundamentals and vocabulary (idt ISO 9000.2000)
YY/T 0287 medical device quality management system for regulatory requirements (YY/T 0287-2003, ISO 13485.2003,
IDT)
3 Terms and Definitions
YY/T 0287 and the following terms and definitions and GB/T 19000-20003.1 established in applicable to this standard.
3.1
The method of any surgically implanted whole or in part, or to rely on the method of implanting the medical intervention body lumen, epithelial or substituted
Ocular surfaces or surfaces; and retained at least 30 days after surgery and the only reliable method of removing a medical intervention or the passive or active treatment
Treatment equipment.
Note. YY/T 0287 in the active implantable medical device is separated from the definition of an implantable medical device out and given a separate definition. The standard fixed
Meaning different from the definition of YY/T 0287, because it will implantable medical devices and active implantable medical devices defined separately into a single definition.
3.2
Implantable medical devices Surgery is performed when the behavior of the following operations.
--- All implanted in the body, or
--- Used to replace an epithelial surface or the surface of the eye, or
--- Portion of the implant body.
Implant surgery retain at least 30d and can only rely on medical or surgical intervention to remove.
YY/T 0682-2008/ISO 16054.2000
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