At Golden, your safety, comfort, and confidence are our top priorities. That’s why every product is an FDA Class II Medical Device – designed to assist persons with chronic physical disablements – and is backed by the highest quality standards in the industry. Every chair undergoes rigorous testing to ensure exceptional performance, reliability, and compliance with global safety and performance standards.
FDA Class II Medical Devices Designed By Golden are intended to assist persons with physical disablements.
1
Model number is verified
2
Fabric color is verified
3
Options are verified (if applicable)
4
Chair is inspected for fabric cleanliness
5
Upholstery is inspected for the direction of nap
6
Upholstery is inspected for seam integrity and holes
7
Any loose threads are trimmed
8
Leg levelers are checked and tightened
9
All frame bolts are tightened
10
Footboard gap verified as even and straight
11
Placement of five French tacks is verified
12
Proper law tags are located and verified
13
Motor clevis pins are locked
14
All wires are wrapped and fastened with tie wraps
15
Lift frame bolts are securely fastened to bottom arms
16
All scissor mechanism bolts are present and tight
17
Poly packs are inspected and no staples are touching the metal frame
18
Chair is inspected for broken, damaged, or missing parts
19
Frame is inspected for split wood
20
Chair is inspected for loose staples
21
Heat function is turned on and tested, when applicable
22
Washer placement, number of washers at motor clevis, and straps are verified
23
Serial number labels are attached to the lift frame and hand control cord
24
Lift and recline buttons are tested for functionality
25
Sleep position is verified
26
Sit position is verified
27
TV position is verified
28
All massage buttons and massage zones are turned on and tested, when applicable
29
Hand control LED lights are observed. Lights are dimmed when not in use and brightened when any button is pressed
30
Up and down arrow buttons for back and footrest are tested for functionality
31
Transformer is plugged in and LED lights (SmartTek®) are checked on the transformer, hand control, and the motor wire
32
Chair is ridden from fully reclined to the full lifted, ensuring smooth and quiet movement
33
While seated, the chair is inspected for the proper foam and fiber regulation, i.e. no bumps or uneven stuffing
34
Proper owner’s manual is added
35
Arm covers are added, when applicable
36
Appropriate hand tags are applied with swift tack gun
37
Model number, model options, serial number, and sales order number are scanned from work order and box tag
38
Motor serial number is scanned
39
Transformer serial number is scanned
40
If the chair passes inspection, it is sent to boxing with the box labels
Product Testing Standards:
- IEC 60601-1-2:2020 (Ed. 4.1) – Home Healthcare Electrical Safety & Performance
- CISPR 11:2015+A1:2016+A2:2019 – Conducted & Radiated Emissions
- IEC 61000-3-2:2005+A1:2008+A2:2009 – Harmonic Current Emissions
- IEC 61000-3-3:2013 – Voltage Fluctuations and Flicker
- IEC 61000-4-2:2008 – Electrostatic Discharge Immunity
- IEC 61000-4-3:2006+A1:2007+A2:2010 – RF Field and Proximity Immunity
- IEC 61000-4-4:2012 – Fast Transient/Burst Immunity
- IEC 61000-4-5:2014 – Surge Immunity
- IEC 61000-4-6:2013 – Conducted RF Immunity
- IEC 61000-4-8:2009 – Magnetic Field Immunity
- IEC 61000-4-11:2004 – Voltage Interruptions and Variations
- IEC 61000-4-39:2017 – Close Proximity Magnetic Field Immunity
- UN 38.3 – Safe Transportation of Lithium Batteries
- UL 962 – Safety of Household and Commercial Furnishings
- IEC 60335-1:2020 – Safety of Household Electrical Appliances
- ISTA 3A – Packaging Durability for Parcel Delivery