Plastic Security Shower Chair Bath Seat Aluminum Swivel Bathtub Seat

• Condition: New
• Customized: Customized
• Certification: ISO, CE, FDA
• Color: White
• Material: Aluminium
• Type: Chair
• Model NO.: HZ-TA507
• Max. Load Capacity (Kg): 120
• Weight (Kg): 7,8
• Depth (Cm): 52
• Width Adjustable 4-Step (Cm): Width Adjustable 4-Step (Cm)
• Height, (Cm): 61
• Seat Depth, (Cm): 40
• Seat Width, (Cm): 41
• Transport Package: Carton
• Specification: Aluminum Swivel frame+ plastic seat
• Trademark: HZ
• Origin: Shanghai
• HS Code: 87131000
• Production Capacity: >10000PCS/Year

Product Description

Product Description

Aluminum Swivel Bathtub Seat

Item Number: HZ-TA507 Composition Powder coated aluminum frame Width adjustable Lockable swivel seat Detachable seat Armrests

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 swivel bathtub seat offers the possibility to cleansing the body while sitting on top of the bathtub. In this way the bathtub can be used without getting in to the bathtub. The swivel function makes it easy to get in to the chair and out of the chair.
Indication
The swivel bathtub seat useful in case of:

• For people with problems to get in to or out of the bathtub.
• People with function failures of the lower extremities
• Patients with a limited control of their trunk

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

• Perception disorders
• Severe imbalance

Technische Daten:
 

Aluminum Swivel Bathtub Seat	HZ-TA507
Max. Load Capacity (kg)	120
Weight (kg)	7,8
Depth (cm)	52
Width adjustable  4-step (cm)	76-86
Height, (cm)	61
Seat Depth, (cm)	40
Seat Width, (cm)	41
Color	white
Frame Seat + Backrest Tips	Powder coated aluminum PE TPE

Packing
1pc / carton
Usage and warnings
Please check the Owner Manual for the usage and any warnings.

MDR (EU) 2017/745 Classification
The HZ-TA507 Swivel Bathtub Seat 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