Rexall

Primary DI
00197344018737
Brand
Rexall
Company
DOLGENCORP, LLC
Model
DG4335
Catalog number
DG4335
Device description
GLOVE, EXAM, VINYL, PF,30CT, OSFM
Published
2025-10-02
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
LYZVinyl Patient Examination Glove

Product Code Classifications#

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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10197344018734PackageGS18In Commercial Distribution
20197344018731PackageGS13In Commercial Distribution
00197344018737PrimaryGS10
80197344018733Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1019734401873410197344018734
2019734401873120197344018731
00197344018737001973440187371973440187370197344018737
8019734401873380197344018733

GMDN Terms#

Term, Definition table
TermDefinition
Vinyl examination/treatment glove, non-powderedA non-sterile device made of vinyl 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 talcum powder and it does not have antimicrobial features. 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.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Protect from freezing . Avoid excessive heat. Product should be shielded from direct sunlight, fluorescent lighting. Keep dry.

Regulatory Flags#

DUNS number
068331990
Device count
30
Lot or batch
true
Manufacturing date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00017276224771Rexall0172762247712020-09-07
00834533001414DG HealthBDGGC362026-03-23
00834533001445DG HealthBDGGS182026-03-23
10834533001411DG HealthBDGGC362026-03-23
10834533001442DG HealthBDGGS182026-03-23
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10751774000037DG Health20002256N/A2026-02-20
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00751774262469DG HealthOne Step Pregnancy TestN/A2025-05-09
00845717090001Rexall77-35277-3522016-09-24
00845717773591Rexall77-35977-3592016-09-24
10751774260479Dollar GeneralOne Step Pregnancy Test2025-05-09
10751774262466DG HealthOne Step Pregnancy TestN/A2025-05-09
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00751774250787DG healthOne Step Pregnancy TestN/A2023-10-27
10751774250784DG healthOne Step Pregnancy TestN/A2023-10-27

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Primary DI, Brand, Company table
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