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YY/T 0003-2023: Manual medical bed
Status: Valid YY/T 0003: Evolution and historical versions
| Standard ID | Contents [version] | USD | STEP2 | [PDF] delivered in | Standard Title (Description) | Status | PDF |
| YY/T 0003-2023 | English | 519 |
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Manual medical bed
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YY/T 0003-2023
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| YY 0003-1990 | English | 279 |
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sickbed
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YY 0003-1990
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PDF similar to YY/T 0003-2023
Standard similar to YY/T 0003-2023 YY/T 0339 YY 0042 YY/T 0490 YY 9706.287 Basic data | Standard ID | YY/T 0003-2023 (YY/T0003-2023) | | Description (Translated English) | Manual medical bed | | Sector / Industry | Medical Device & Pharmaceutical Industry Standard (Recommended) | | Classification of Chinese Standard | C46 | | Classification of International Standard | 11.040.99 | | Word Count Estimation | 26,271 | | Date of Issue | 2023-11-22 | | Date of Implementation | 2025-12-01 | | Older Standard (superseded by this standard) | YY/T 0003-1990 | | Issuing agency(ies) | State Drug Administration | | Summary | This standard specifies the requirements, test methods and instructions for manual hospital beds. This standard applies to manual hospital beds. This product is intended for use in patients with a height equal to or greater than 146cm, a mass equal to or greater than 40kg, and a body mass index (BMI) equal to or greater than 17. | YY/T 0003-2023: Manual medical bed---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
ICS 11.040.99
CCSC46
Pharmaceutical Industry Standards of the People's Republic of China
Replaces YY/T 0003-1990
Manual Bed
Released on 2023-11-22
2025-12-01 Implementation
The State Drug Administration issued
Table of Contents
Preface III
1 Scope 1
2 Normative references 1
3 Terms and Definitions 1
4 Requirement 3
4.1 Angle 3
4.2 Preventing the patient from being trapped by non-moving parts 5
4.3 Strength requirements for patient or operator support or suspension systems 8
4.4 Instability-Imbalance 8
4.5 Pushing force 8
4.6 Sidebar Strength and Latch Reliability 9
4.7 Preventing patients from accidentally falling 9
4.8 Rough handling 10
4.9 Headboard/footboard assembly 10
4.10 Operating device 10
4.11 Requirements for manual beds 10
4.12 Annex 10
4.13 Appearance 10
4.14 Logo 10
5 Test methods 12
5.1 Angle 12
5.2 Preventing patients from being trapped by non-moving parts12
5.3 Strength requirements for patient or operator support or suspension systems 13
5.4 Instability-Imbalance 15
5.5 Pushing force 18
5.6 Sidebar Strength and Latch Reliability 18
5.7 Preventing patients from accidentally falling 19
5.8 Rough handling 19
5.9 Headboard/footboard assembly 19
5.10 Operating device 19
5.11 Requirements for manual beds 19
5.12 Annex 19
5.13 Appearance 20
5.14 Logo 20
6 Instructions 20
Reference 21
Foreword
This document is in accordance with the provisions of GB/T 1.1-2020 "Guidelines for standardization work Part 1.Structure and drafting rules for standardization documents"
Drafting is required.
This document replaces YY/T 0003-1990 "Hospital Beds". Compared with YY/T 0003-1990, except for structural adjustments and editorial changes,
In addition, the main technical changes are as follows.
--- Added terminology items and related definitions (see Chapter 3, Chapter 3 of the.1990 edition);
--- Changed the angle requirements (see 4.1, 3.4 of the.1990 edition);
--- Changed the strength requirements (see 4.3, 4.8 and 4.9 of the.1990 edition);
--- Added "preventing patients from falling accidentally" and changed the height of the bed rails (see 4.7, 4.16.4 of the.1990 edition);
--- Added technical requirements "prevent patients from being trapped by non-moving parts" (see 4.2), "instability" (see 4.4), "driving force" (see
4.5), "Sidebar strength and latch reliability" (4.6), "Identification" (4.14);
--- Changed the "operating device" requirements (see 4.10, 4.7 of the.1990 edition);
--- Changed the coordination requirements for manual beds (see 4.11, 4.5 of the.1990 edition);
--- Changed the requirements for the appendix (see 4.12, 4.16 of the.1990 edition);
--- The test method has been changed (see Chapter 5, Chapter 5 of the.1990 edition);
--- Added relevant requirements for instructions (see Chapter 6);
--- Deleted the classification (see Chapter 3 of the.1990 edition);
--- Deleted the inspection rules (see Chapter 6 of the.1990 edition);
--- Deleted marking, packaging, transportation and storage (see Chapter 7 of the.1990 edition);
--- Deleted the warranty period (see Chapter 8 of the.1990 edition).
Please note that some of the contents of this document may involve patents. The issuing organization of this document does not assume the responsibility for identifying patents.
This document is proposed by the State Food and Drug Administration.
This document is provided by the National Technical Committee for Standardization of Medical Electrical Appliances, Medical Electronic Instruments Standardization Subcommittee (SAC/TC10/SC5)
Centralized.
This document was drafted by. Guangdong Medical Device Quality Supervision and Inspection Institute, Shanghai Medical Device Inspection Institute, Balemeng Bed Industry
(China) Co., Ltd., Kaitai Medical Equipment Co., Ltd.
The main drafters of this document. Suning, Zhou Jiajie, Liu Zhenzhen, Xu Chao, Zhuang Jun, Gao Zhiwei, Hu Changming, Ye Shasha, Liang Yi.
The previous versions of this document and the documents it replaces are as follows.
---First published in.1990 as YY 0003-1990;
---This is the first revision.
Manual Bed
1 Scope
This document specifies the requirements, test methods and instructions for manual hospital beds.
This document applies to manual beds. This product is intended for use with a height of 146 cm or more, a mass of 40 kg or more, and a weight of
Patients with a BMI equal to or greater than 17.
2 Normative references
This document has no normative references.
3 Terms and definitions
The following terms and definitions apply to this document.
3.1
Patient
People who are receiving treatment.
[Source. YY 9706.252-2021,.201.3.76, modified]
3.2
In hospitals that provide intensive care, 24-hour medical supervision or continuous monitoring is required, and the use of biological
A place where life support systems/equipment are used to maintain or enhance patient function.
[Source. YY 9706.252-2021,.201.3.201]
3.3
In hospitals or other medical institutions providing emergency care, medical supervision and monitoring are required and are often used during medical procedures.
A place where medical equipment is used to maintain or improve a patient's condition.
[Source. YY 9706.252-2021,.201.3.202]
3.4
There are areas with long-term care, where medical supervision and monitoring are required and where necessary, where medical care may be used during the course of treatment.
A place where equipment is used to maintain or improve a patient's condition.
Note. Includes use in nursing homes, rehabilitation facilities and facilities for the elderly.
[Source. YY 9706.252-2021,.201.3.203]
3.5
A place in the home where care is provided where medical equipment is used to relieve or compensate for injury, disability, or illness.
NOTE. When a manual bed is designed solely for use in application environment 4, all other application environments (e.g. nursing homes, rehabilitation facilities and facilities for the elderly) are excluded.
[Source. YY 9706.252-2021,.201.3.204, modified]
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