Condition: | New |
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Customized: | Customized |
Certification: | ISO, CE, FDA |
Folded: | Non-Folding |
Application: | Elderly, Pregnant Woman, Patient People |
Characteristic: | Multi-Function, Design Sense, Resistance to Heavy, Fashion, Beautiful |
Samples: |
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Customization: |
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Introducing the Health Care Commode Chair for Patient Care by Shanghai Haozheng Metal Products Co., Ltd. This portable and hygienic commode chair is designed to provide assistance to elderly patients and those with mobility issues. It serves as a toilet aid and patient care chair, offering comfort and convenience at home or in healthcare settings. The sturdy construction and compact design make it an ideal choice for senior care and patient toileting. Choose this assistive device commode for reliable and efficient patient assistance.
Item Number: HZ-CC102 Composition
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Users with limited mobility but sufficient sitting ability.
Designed for indoor and stationary use only.
The commode chair is essential for individuals who are unable to reach or use the toilet due to their disability.
The device is suitable for:
The commode chair should not be used in cases of:
Manufacturer: Shanghai Haozheng Metal Products Co., Ltd.
HZ-CC102 | |
Max. Load Capacity (kg) | 130 |
Weight (kg) | 8 |
Total width (cm) | 56 |
Height (cm) | 80-95 |
Depth (cm) | 52-57 |
Seat width (cm) | 43 |
Seat depth (cm) | 42 |
Seat height (cm) | 40-55 |
color | blue, black,red |
Size of toilet opening (cm) | 24 x 21 |
Frame Seat Tips Bucket |
Powder coated steel Wood+Foam+PVC TPE PP |
The HZ-CC102 Commode Chair, manufactured by Shanghai Haozheng Metal Products Co., Ltd., is a versatile and reliable medical product designed to provide comfort and convenience for individuals with mobility issues.
For detailed instructions on how to use the Commode Chair and important safety warnings, please refer to the Owner Manual provided with the product.
The HZ-CC102 Commode Chair is classified as a Class I medical product under the EU-Regulation MDR 2017/745. This classification is based on Rule 1, Annex VIII, Chapter III of the Regulation MDR (EU) 2017/745.
Test institute / facility | |
Test Standard | ISO 12182 |
Test Certificate / Number | |
Date of test |
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