Commode Chair Paitent Chair Toilet Aids Chair

• Condition: New
• 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
• Model NO.: HZ-CC102
• Material: Steel
• Max. Load Capacity (Kg): 130
• Weight (Kg): 8
• Total Width (Cm): 56
• Height (Cm): 80-95
• Color: Blue, Black,Red
• Transport Package: Carton
• Trademark: HZ
• Origin: China
• HS Code: 87131000
• Production Capacity: >10000PCS/Year

Product Description

Product Description

Stacking Commode Chair

Item Number: HZ-CC102 Composition Powder coated steel frame Height adjustable Waterproofed vinyl seat and backrest cover Padded seat and backrest Toilet bucket under the seat

Characterization of the user or patient
Users with a limited possibility of movement, but with a sufficient sitting ability.
Characterization of the environment of use
Indoor and stationary areas usage only

Intended use
The commode chair is necessary, if reaching the toilet, or the use of the toilet is no longer possible due to the disability

Indication
The device is useful in case of:

• Patients with a limited control of their trunk
• People with impaired balance, vertigo
• People with function failures of the lower extremities
• Significantly restricted mobility of the lumber spine, the hip and the knee joints
• Paralysis

Contraindication
The commode chair should not be used in case of:
 

• Perception disorders
• Severe imbalance

Technical Details:
 

	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

Packing
Stacked / 3-5pcs / carton

Usage and warnings
Please check the Owner Manual for the usage and any warnings.





MDR (EU) 2017/745 Classification
The HZ-CC102 Commode Chair is classified under the EU-Regulation MDR 2017/745 as a Class I medical product.
The classification is based on Rule 1, Annex VIII, Chapter III of the Regulation MDR (EU) 2017/745.

Product Testing

Test institute / facility
Test Standard	ISO 12182
Test Certificate / Number
Date of test