FDA.reportPublic FDA data

Wavy Donning Gloves

Primary DI
00745129215293
Brand
Wavy Donning Gloves
Company
SIGVARIS INC
Model
590R
Catalog number
590RPRM
Device description
A device made of natural latex intended to assist patients and caregivers in donning and removing compression stockings and garments without causing damage to the stocking (e.g. from nails, jewelry). This device will have appropriate characteristics regarding tactility/comfort of use, and should provide appropriate physical properties (e.g., strength, elasticity), and uniformity of dimensions. This is a single-use device.
Published
2016-12-05
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
IKXAid, Transfer

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
IKXAid, TransferPhysical Medicine1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00745129184346PackageGS112Not in Commercial Distribution
00745129215293PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00745129184346007451291843467451291843460745129184346
00745129215293007451292152937451292152930745129215293

GMDN Terms#

Term, Definition table
TermDefinition
Compression/pressure sock/stocking, single-useA garment in the form of a sock or stocking intended to fit tightly over the leg and foot to apply compression/pressure (i.e., graduated or even-force), typically for the treatment/prevention of a disorder(s) of circulation [e.g., venous insufficiency, deep vein thrombosis (DVT)]. It is not a strip/roll binder or tubular support bandage, and is not designed to cover the pelvis. It is typically made of elastic material (e.g., circular knit nylon/Spandex yarns) and may be referred to as a flight sock; it does not include antimicrobial features. It is intended for use in the home or a clinical setting. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Contacts#

Phone, Email table
PhoneEmail
+1(800)322-7744sigvariscares@sigvaris.com

Regulatory Flags#

DUNS number
189738719
Device count
1
Premarket exempt
true
Lot or batch
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
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07613378196553862T-CUSTOM ECF2 AG SoftTop UNI Black3205633205632026-05-18
07613378196560862N-CUSTOM ECF2 AG SensinovaUnisex UNI Black3205623205622026-05-18
07613378196942862T-CUSTOM ECF2 AG SoftTop UNI °° Caramel3205243205242026-05-18
07613378197338862T-CUSTOM ECF2 AG SoftTop UNI Caramel3204853204852026-05-18
07613378197345862N-CUSTOM ECF2 AG SensinovaUnisex UNI Caramel3204843204842026-05-18
07613378197727862T-CUSTOM ECF2 AG SoftTop UNI °° Grey3204463204462026-05-18
07613378198113862T-CUSTOM ECF2 AG SoftTop UNI Grey3204073204072026-05-18
07613378198120862N-CUSTOM ECF2 AG SensinovaUnisex UNI Grey3204063204062026-05-18
07613378198502862T-CUSTOM ECF2 AG SoftTop UNI °° Savanna3203683203682026-05-18
07613378198892862T-CUSTOM ECF2 AG SoftTop UNI Savanna3203293203292026-05-18
07613378198908862N-CUSTOM ECF2 AG SensinovaUnisex UNI Savanna3203283203282026-05-18
07613378199288862T-CUSTOM ECF2 AG SoftTop UNI °° Skin3202903202902026-05-18
07613378199677862T-CUSTOM ECF2 AG SoftTop UNI Skin3202513202512026-05-18
07613378199684862N-CUSTOM ECF2 AG SensinovaUnisex UNI Skin3202503202502026-05-18
07613378277504862N-CUSTOM ECF2 AG SensinovaUnisex UNI marine3555233555232026-05-18
07613378277511862T-CUSTOM ECF2 AG SoftTop UNI marine3555243555242026-05-18
07613378277900862T-CUSTOM ECF2 AG SoftTop UNI °° marine3555633555632026-05-18
00745129334581422C Motion Thermo Wool 20-30mmHG U LL Denim MSTRP422CLL39 or 22061422CLL392026-05-11

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