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YY 0285.1-2017

Chinese Standard: 'YY 0285.1-2017'
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BASIC DATA
Standard ID YY 0285.1-2017 (YY0285.1-2017)
Description (Translated English) Intravascular catheters--Sterile and single-use catheters--Part 1: General requirements
Sector / Industry Medical Device & Pharmaceutical Industry Standard
Classification of Chinese Standard C31
Classification of International Standard 11.040.20
Word Count Estimation 26,251
Date of Issue 2017-07-17
Date of Implementation 2019-01-01
Older Standard (superseded by this standard) YY 0285.1-2004
Drafting Organization Shanghai Medical Device Testing Institute, Beilang Medical (Shanghai) International Trade Co., Ltd., Shanghai Minimally Invasive Medical Devices (Group) Co., Ltd.
Administrative Organization State Food and Drug Administration, Jinan Medical Device Quality Supervision and Inspection Center
Proposing organization China Food and Drug Administration
Issuing agency(ies) State Food and Drug Administration

YY 0285.1-2017
PHARMACEUTICAL INDUSTRY STANDARD
OF THE PEOPLE’S REPUBLIC OF CHINA
ICS 11.040.20
C 31
Replacing YY 0285.1-2004, YY 0285.2-1999
Intravascular catheters - Sterile and single-use catheters
- Part 1. General requirements
血管内导管 一次性使用无菌导管
第 1部分.通用要求
(ISO 10555-1.2013, MOD)
ISSUED ON. JULY 17, 2017
IMPLEMENTED ON. JANUARY 1, 2019
Issued by. China Food and Drug Administration
Table of Contents
Foreword ... 3 
1 Scope ... 5 
2 Normative references ... 5 
3 Terms and definitions ... 6 
4 Requirements ... 9 
5 Logo of nominal size ... 11 
6 Information provided by manufacturers ... 12 
Foreword
YY 0285 “Intravascular catheters - Sterile and single-use catheters” consists of four
parts.
- Part 1. Intravascular catheters - Sterile and single-use catheters - Part 1.
General requirements;
- Part 3. Intravascular catheters - Sterile and single-use catheters - Part 3. Central
venous catheters;
- Part 4. Intravascular catheters - Sterile and single-use catheters - Part 4. Balloon
dilatation catheters;
- Part 5. Intravascular catheters - Sterile and single-use catheters - Part 5. Trocar
peripheral catheter.
This part is the first part of YY 0285.
This part was drafted in accordance with the rules in GB/T 1.1-2009.
This part replaces YY 0285.1-2004 "Sterile, single-use intravascular catheters. Part
1. General requirements" and YY 0285.2-9 "Sterile, single-use intravascular
catheters - Part 2. Angiographic catheter."
Compared with YY 0285.1-2004 and YY 0285.2-1999, the main technical changes in
this part are as follows.
- revise the requirements and test methods of angiographic catheter;
- revise flow requirements;
- modify some verbal expressions. This part uses the redrafted law revision using
IS0 10555-1. 2013 "Intravascular catheters - Sterile and single-use catheters -
Part 1. General requirements".
The technical differences and the reasons between this part and ISD 10555-1. 2013
are as follows.
- With regard to the normative references, this part has made adjustments with
technical differences so as to adapt to the technical conditions in our country.
The adjustments are mainly reflected in Chapter 2 "Normative References". The
specific adjustments are as follows.
• Replace ISD 594-1 with identical international standard GB/T 1962.1;
Intravascular catheters - Sterile and single-use catheters
- Part 1. General requirements
1 Scope
This part of YY 0285 specifies the general requirements for Intravascular catheters
of various uses with sterile supply and single-use. This part does not apply to
Intravascular catheter accessories, such as YY 0450.1.
2 Normative references
The following document for the application of this document is essential. For dated
references, only the dated version applies to this document. For undated references,
the latest edition (including all amendments) applies to this document.
GB/T 1962.1 Conical fittings with a 6% (Luer) taper for syringes, needles and certain
other medical equipment. Part 1. General requirement (GB/T 1962.1-2015, ISO
594-1. 1986, IDT)
GB/T 1962.2 Conical fittings with a 6% (Luer) taper for syringes, needles and certain
other medical equipment. - Part 2. Locking joints (ISO/IEC 1962.2-2001, ISO 594-2.
1998, IDT)
GB 15810 Sterile hypodermic syringes for single-use (GB15810-2001, eqv ISO
7886-1. 1993)
GB/T 30515 Petroleum products. Transparent and opaque liquids. Determination of
kinematic viscosity and calculation of dynamic viscosity (GB/T 30515- 2014, ISO
3104.1994, MOD)
YY/T 0466.1 Medical devices. Symbols to be used with medical device labels,
labelling and information to be supplied. Part 1. General requirements (YY/T
0466.1-2016, ISO 5223-1.2012, IDT)
YY/T 0586 Medical polymer products-Test methods of radiopacity
ISO 3105.1994 Glass capillary kinematic viscometers. Specifications and operating
instructions second edition (Glass capillary kinematic viscometers-Specifications and
operating instructions)
3.7
Outside diameter
It is the maximum diameter of a catheter or hydration catheter that can be inserted
into blood vessel in ante-hydration and post-hydration.
3.8
Junction
It is the connection of one or more pipelines where the pipe connections are capable
of withstanding mechanical tension or mechanical stress during clinical use.
3.9
Hydratable intravascular catheter
Intravascular catheters that contain a material that exhibits clinically significant
hydration after touch an aqueous medium.
3.10
Post-hydration
The hydratable intravascular catheter is immersed into (37 ± 2) ° C water and
maintained for the state after the clinically expected period of use.
3.11
Clinically significant hydration
The effective length of post-hydration is 1% greater than the effective length of
ante-hydration, or the outside diameter of post-hydration is 10% greater than or
equal to the outside diameter of ante-hydration.
3.12
Power injection
It is the rapid injection of liquid under high pressure.
3.13
Primary packaging
It is the packaging that directly contacts with instruments and / or keep products
sterile.
mm, the flow of each cavity shall be no less than 80% of the nominal value of
manufacturers; as for the catheter having a nominal outside diameters greater than
or equal to 1.0 mm, the flow of each cavity shall be no less than 90% of the nominal
value of manufacturers. If measuring the flow of hydration catheter, the
post-hydration flow shall be measured.
4.10 Power injection
If the catheter is marked for power injection, the burst pressure measured in
accordance with Appendix F shall be greater than the peak pressure at the
maximum flow measured in accordance with Appendix G.
4.11 Side hole
The design, number and position of side holes shall minimize adverse effects on the
catheter and damage to the tissue.
4.12 Distal end & head end
To reduce damage to the blood vessels during use, the distal end & head end of the
catheter shall be rounded, tapered or treated similarly.
5 Logo of nominal size
5.1 General rules
The nominal size of the catheter shall be identified as specified in 5.1 and 5.2.
5.2 Outside diameter
Unless otherwise specified in the standard for a particular type of catheter, the
outside diameter shall be expressed in millimeters1) and sent to the nearest 0.01 mm
or 0.1 mm.
For the instrument whose cross-section designs non-circular, the specifications shall
be marked with the maximum shaft diameter. In this case, the manufacturer may
choose to provide additional information related to the profile of the instrument, such
as the minor axis dimension of the elliptical section.
5.3 Nominal effective length
When effective length is less than 100 mm, it shall be expressed in millimeters; when
effective length is greater than or equal to 100 mm, it shall be expressed in
millimeters or centimeters.
1 Appendix H shows the measurement unit system which can be additionally used except for the
provisions of this section.
Appendix B
(Normative)
Peak tension test method
B.1 Principle
Select the test section of the catheter or entire catheter so that each connection
between each tubular portion, catheter adapter or connector and the pipeline, and
connections between each tubular portion are tested. Put tension on each test
section until the pipeline is broken or the connection is separated. When testing
hydration catheters, consider the state of ante-hydration and post-hydration, report
the worst outcome.
B.2 Instrument
Tension tester can exert a force greater than 15N.
B.3 steps
B.3.1 Assemble the catheter according to the manufacturer's instructions. The test is
carried out by selecting a section of the catheter under test, including the hub or the
connector (if any) and the connections between the sections, for example, the
connection between the pipeline and the end-head end. The end-head end with less
than 3mm in length shall not be included in the test section. For hydration catheters,
prepare the test specimen of the same position from both catheters. One specimen
is adjusted according to B.3.2, another specimen is not adjusted but conducted
directly according to B.3.3 ~ B.3.8.
B.3.2 Place the test specimen in a suitable aqueous medium, keep the temperature
of (37 ± 2) °C to the corresponding clinical use of time (see B.3.1), conduct the state
adjustment, and then conduct a test immediately according to B3.3 ~ B.3.8.
B.3.3 Fix the test section to the tension tester, if hub or connector is available, use
appropriate clamps to prevent the hub or the connector from deforming.
B.3.4 Measuring the gauge length of the test section, that is, the distance of test
section among the fixtures of tension tester, or the distance between the hub or
connector and the......
Related standard:   YY 0285.5-2018  YY 0285.3-2017
Related PDF sample:   YY 0285.5-2018
   
 
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