Velvet Touch

Primary DI
00850053649165
Brand
Velvet Touch
Company
Mrglovz.com LLC
Model
Large
Device description
Latex Examination Powder Free Gloves - Large
Published
2023-06-20
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true
Single use
true

Product Codes#

Code, Name table
CodeName
LYYLatex Patient Examination Glove

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LYYLatex Patient Examination GloveGeneral Hospital1

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K202377000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K202377000Palm Care Latex Examination Powder Free GlovesHi-Care Thai Gloves Co. , Ltd.2020-12-01LYY

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850053649172PackageGS110In Commercial Distribution
00850053649165PrimaryGS10
00850053649127Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850053649172008500536491728500536491720850053649172
00850053649165008500536491658500536491650850053649165
00850053649127008500536491278500536491270850053649127

GMDN Terms#

Term, Definition table
TermDefinition
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobialA device made of Hevea natural rubber latex (NRL) intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes; its inner surface is not covered with powder and it does not include antimicrobial agents/materials. The device is used mainly as a two-way barrier to protect both the patient and the staff against various contamination. It 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.

Regulatory Flags#

DUNS number
127613863
Device count
100
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true
Contains natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850053649011Velvet TouchMedium2023-06-20
00850053649035Velvet TouchLarge2023-06-20
00850053649059Velvet TouchXtra-Large2023-06-20
00850053649097Velvet TouchSmall2023-06-20
00850053649134Velvet TouchMedium2023-06-20
00850053649189Velvet TouchExtra Large2023-06-20
00850053649202Velvet TouchSmall2023-06-20
00850053649233Velvet TouchMedium2023-06-20
00850053649226Velvet TouchLarge2023-06-20
00850053649073Velvet TouchXtra-Large2023-06-20
00850053649110Velvet TouchSmall2023-06-20
00850053649158Velvet TouchMedium2023-06-20
00850053649172Velvet TouchLarge2023-06-20
00850053649196Velvet TouchExtra Large2023-06-20
00850053649219Velvet TouchSmall2023-06-20

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
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10076490456556TOUCHNTUFFAnsell Healthcare ProductLYY2025-07-30
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09555002101077AURELIA VIBRANTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101084AURELIA VIBRANTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
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09555002101411AURELIA DISTINCTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101428AURELIA DISTINCTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101435AURELIA DISTINCTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101442AURELIA DISTINCTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
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09555002101565AURELIA REFRESHSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101572AURELIA REFRESHSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101589AURELIA REFRESHSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101596AURELIA REFRESHSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
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