FDA.report

Ultragard

Primary DI
00816928026318
Brand
Ultragard
Company
Ultragard
Model
V300-S
Device description
box of 100 powder free vinyl examination gloves, non-sterile, size Small
Published
2025-02-03
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
true

Related Records

Product Codes

CodeName
LYZVinyl Patient Examination Glove

Product Code Classifications

CodeDeviceSpecialtyClass
LYZVinyl Patient Examination GloveGeneral Hospital1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00816928026318PackageGS110In Commercial Distribution
00816928021313PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00816928026318008169280263188169280263180816928026318
00816928021313008169280213138169280213130816928021313

GMDN Terms

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.

Sterilization Methods

Method

Regulatory Flags

DUNS number
175840941
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company

Primary DIBrandModelCatalogPublished
00816928026325UltragardV300-M2025-02-03
00816928026332UltragardV300-L2025-02-03
00816928026349UltragardV300-XL2025-02-03
00816928027711UltragardB300-S2025-02-03
00816928027728UltragardB300-M2025-02-03
00816928027735UltragardB300-L2025-02-03
00816928027742UltragardB300-XL2025-02-03
00816928027506UltragardN300-XS2024-03-19
00816928027551UltragardN300-XXL2024-03-19
00816928025250UltragardUGET-XXL2023-10-10
00816928025601UltragardUGNTPF-XS2023-05-25
00816928025618UltragardUGNTPF-S2023-05-25
00816928025625UltragardUGNTPF-M2023-05-25
00816928025632UltragardUGNTPF-L2023-05-25
00816928025649UltragardUGNTPF-XL2023-05-25
00816928028008UltragardL300-XS2023-05-25
00816928028015UltragardL300-S2023-05-25
00816928028022UltragardL300-M2023-05-25
00816928028039UltragardL300-L2023-05-25
00816928028046UltragardL300-XL2023-05-25

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