FDA.reportPublic FDA data

Handi-Move Wall Lift

Primary DI
05404016610416
Brand
Handi-Move Wall Lift
Company
Handi-Move
Model
2422 00000001
Device description
Wall Lift Heavy Duty 110V
Published
2020-09-01
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
FNGLIFT, PATIENT, AC-POWERED

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FNGLift, Patient, Ac-PoweredGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05404016610416PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05404016610416054040166104165404016610416

GMDN Terms#

Term, Definition table
TermDefinition
Stationary patient lifting system, line-poweredA mains electricity (AC-powered), stationary assembly of devices designed to enable one person to lift and move an incapacitated patient or a person with a disability, of any size and weight, safely and with minimal physical effort within an area limited by the lifting radius of the system. Also known as a patient hoist, it typically consists of a support base fixed permanently to a ceiling, wall, floor, or piece of equipment such as a bath or the edge of a swimming pool, with a motorized lifting mechanism, mast, boom/lifting arm(s), swivel bar, and patient holding device (e.g., a sling, holder or a frame).

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800) 724-5305info@surehands.com

Regulatory Flags#

DUNS number
283658730
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
05404016612250Handi-Move Sling3517L 900000013517L 900000012020-10-20
05404016612274Handi-Move Sling3517M 900000013517M 900000012020-10-20
05404016612298Handi-Move Sling3517S 900000013517S 900000012020-10-20
05404016612311Handi-Move Sling3517XL 900000013517XL 900000012020-10-20
05404016612335Handi-Move Sling3517XS 900000013517XS 900000012020-10-20
05404016612342Handi-Move Sling3522L 900000013522L 900000012020-10-20
05404016612359Handi-Move Sling3522M 900000013522M 900000012020-10-20
05404016612366Handi-Move Sling3522S 900000013522S 900000012020-10-20
05404016612373Handi-Move Sling3522XL 900000013522XL 900000012020-10-20
05404016612380Handi-Move Sling3522XS 900000013522XS 900000012020-10-20
05404016611918Handi-Move Sling3489M 900000013489M 900000012020-10-12
05404016611321Handi-Move Sling3461L 900000013461L 900000012020-09-30
05404016611345Handi-Move Sling3461M 900000013461M 900000012020-09-30
05404016611369Handi-Move Sling3461S 900000013461S 900000012020-09-30
05404016611383Handi-Move Sling3461XL 900000013461XL 900000012020-09-30
05404016611406Handi-Move Sling3461XS 900000013461XS 900000012020-09-30
05404016610744Handi-Move Sling3415L 000000013415L 000000012020-09-08
05404016610751Handi-Move Sling3415L 900000013415L 900000012020-09-08
05404016610768Handi-Move Sling3415M 000000013415M 000000012020-09-08
05404016610775Handi-Move Sling3415M 900000013415M 900000012020-09-08

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