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YY/T 0980.3-2016 English PDF

YY/T 0980.3-2016 (YY/T0980.3-2016, YYT 0980.3-2016, YYT0980.3-2016)
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YY/T 0980.3-2016English140 Add to Cart 0--9 seconds. Auto-delivery Biopsy needles for single use. Part 3: Mechanical assembly type Valid YY/T 0980.3-2016

Standard ID YY/T 0980.3-2016 (YY/T0980.3-2016)
Description (Translated English) Biopsy needles for single use -- Part 3: Mechanical assembly type
Sector / Industry Medical Device & Pharmaceutical Industry Standard (Recommended)
Classification of Chinese Standard C31
Word Count Estimation 10,118
Date of Issue 2016-07-29
Date of Implementation 2017-06-01
Quoted Standard GB/T 1220; GB/T 2965; YY/T 0980.1-2016
Drafting Organization Zhejiang Voltte Medical Devices Co., Ltd., Shanghai Medical Devices Testing Co., Ltd., Shanghai Es Egyptian Medical Plastic Products Co., Ltd.
Administrative Organization National Medical Syringe (Needle) Standardization Technical Committee (SAC/TC 95)
Regulation (derived from) State Food and Drug Administration Notice 2016 (No.129)
Proposing organization State Administration of Food and Drug Administration
Issuing agency(ies) State Administration of Food and Drug Administration
Summary This standard specifies the requirements for a one-time use of a biopsy needle - a motorized assembly (hereinafter referred to as a "biopsy needle"). This standard applies to disposable needle body and reusable mechanical power devices assembled together, with mechanical power device for automatic or semi-automatic cutting operation to collect live tissue samples of the disposable use of motorized biopsy needle. This standard does not apply to reusable biopsy needles and mechanical power devices that are connected to the biopsy needle by means of assembly.

Standards related to: YY/T 0980.3-2016

YY/T 0980.3-2016
ICS 11.040.20
C 31
Biopsy needles for single use -
Part 3. Mechanical assembly type
ISSUED ON. JULY 29, 2016
Issued by. China Food and Drug Administration
3. No action is required - Full-copy of this standard will be automatically &
immediately delivered to your EMAIL address in 0~60 minutes.
Table of Contents
Foreword ... 3
Introduction ... 4
1 Scope ... 5
2 Normative references ... 5
3 Structure type... 5
4 Material ... 7
5 Requirements and test methods ... 7
6 Packaging and marking ... 9
7 Instructions for use ... 10
8 Transportation and storage ... 10
9 Type inspection rules ... 10
Annex A (informative) Type inspection rules ... 11
Bibliography ... 12
YY/T 0980 “Biopsy needles for single use” series of standards consist of the following
- Part 1. General requirements;
- Part 2. Manual biopsy needle;
- Part 3. Mechanical assembly type
- Part 4. Mechanical complete type.
This Part is Part 3 of YY/T 0980 “Biopsy needles for single use”.
This Part is drafted in accordance with the rules given in GB/T 1.1-2009.
Attention is drawn to the possibility that some of the elements of this document may
be the subject of patent rights. Issuing organizations of this document shall not be held
responsible for identifying any or all such patent rights.
This Part is proposed by China Food and Drug Administration.
This Part is under the jurisdiction of National Technical Committee on Medical Syringes
(Needles) of Standardization Administration of China (SAC/TC 95).
Main drafting organizations of this Part. Zhejiang Fert Medical Device Co., Ltd.,
Shanghai Testing & Inspection Institute for Medical Devices, Shanghai SA Medical &
Plastic Instruments Co., Ltd.
Main drafters of this Part. Su Weidong, Wang Zewei, Cao Xianming.
This Part does not provide requirements and methods for sampling performance and
ultrasonic development, because currently there is no suitable test methods and
simulation test materials.
In view of the fact that the structure type of mechanical assembly type biopsy needles
and the location, depth, state, texture and method of the puncture are different, this
Part does not specify the puncture force. However, manufacturers are encouraged to
determine appropriate puncture force by verifying, combining the specific structure and
use of the mechanical assembly type biopsy needle produced by each of the
Biopsy needles for single use -
Part 3. Mechanical assembly type
1 Scope
This Part of YY/T 0980 specifies the requirements for biopsy needles for single use -
mechanical assembly type (hereinafter referred to as “biopsy needles”).
This Part applies to mechanical assembly type biopsy needles for single use, which
consist of needles for single use and reusable mechanical power devices for automatic
or semi-automatic cutting operations to collect biopsy samples.
This Part does not apply to reusable biopsy needles and mechanical power devices
connected with the biopsy needle by means of assembly before use.
2 Normative references
The following referenced documents are indispensable for the application of this
document. For dated references, only the edition cited applies. For undated references,
the latest edition of the referenced document (including any amendments) applies.
GB/T 1220 Stainless steel bar
GB/T 2965 Titanium and titanium alloy bar
YY/T 0980.1-2016 Biopsy needles for single use - Part 1. General requirements
3 Structure type
3.1 A biopsy needle consists of an outer needle tube, an outer needle seat, an inner
needle bar, an inner needle seat, a fixed part and a protective cover.
NOTE. Biopsy needles can be used with guide needles, cursors, etc. when necessary.
7 Instructions for use
The instructions for use shall have at least the following information.
a) product name;
b) product model description;
c) product performance, main structure;
d) use methods and precautions;
e) storage conditions;
f) prompt information that it can be equipped with mechanical power device;
g) other instructions and necessary warnings.
8 Transportation and storage
8.1 During transportation and storage process, biopsy needles shall be prevented from
stress, sun and rain and snow.
8.2 Biopsy needles shall be stored in a non-corrosive-gas, well ventilated and clean
9 Type inspection rules
See Annex A for type inspection rules.