FDA.reportPublic FDA data

VGUARD

Primary DI
00810052977232
Brand
VGUARD
Company
Vanguard International Solutions, LLC
Model
A11A10
Device description
Nitrile Exam PF Blue 10/100 XS
Published
2024-09-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Single use
true

Product Codes#

Code, Name table
CodeName
LZAPolymer Patient Examination Glove

Product Code Classifications#

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K092874000
K131440000
K210684000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K092874000POWDER FREE NITRILE (DARK BLUE) EXAMINATION GLOVESQuality Gallant Sdn. Bhd.2010-06-22LZA
K131440000POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUEHebei Hongsen Plastics Technology Co, Ltd.2013-09-25LZA
K210684000Disposable Nitrile Medical Examination GloveJiangsu Cureguard Glove Co., Ltd.2021-07-20LZA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810052977249PackageGS1100In Commercial Distribution
00810052977256PackageGS110In Commercial Distribution
00810052977232PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810052977249008100529772498100529772490810052977249
00810052977256008100529772568100529772560810052977256
00810052977232008100529772328100529772320810052977232

GMDN Terms#

Term, Definition table
TermDefinition
Nitrile examination/treatment glove, non-powdered, non-antimicrobialA device made of nitrile 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 patient/staff against contaminants and risk of allergy to latex. It will have appropriate characteristics regarding tactility and comfort of use, and should provide appropriate physical properties (e.g., tensile strength, resistance to puncture, elasticity), and uniformity of dimensions (i.e., sizing consistency). This is a single-use device.

Regulatory Flags#

DUNS number
093129027
Device count
1
Lot or batch
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810052977522VGUARDA11A152024-09-22
00810052977249VGUARDA11A102024-09-22
00810052977539VGUARDA11A152024-09-22
00810073734777Wise Choice520212024-08-23
00810073734807Wise Choice520222024-08-23
00810073734838Wise Choice520232024-08-23
00810073734869Wise Choice520242024-08-23
00810073734784Wise Choice520212024-08-23
00810073734814Wise Choice520222024-08-23
00810073734845Wise Choice520232024-08-23
00810073734876Wise Choice520242024-08-23
00810073732957VGUARDA16A302024-08-08
00810073734890Wise Choice341012024-08-08
00810073734920Wise Choice341022024-08-08
00810073734951Wise Choice341032024-08-08
00810073734982Wise Choice341042024-08-08
00810073732964VGUARDA16A302024-08-08
00810073734906Wise Choice341012024-08-08
00810073734937Wise Choice341022024-08-08
00810073734968Wise Choice341032024-08-08

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Primary DI, Brand, Company table
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