VIVIT

Primary DI
10810084210199
Brand
VIVIT
Company
1. Vivit International Inc
Model
20521
Device description
Nitrile Examination Glove, Powder-Free, Textured Fingertips, Chemotherapy Drug Tested, Purple, X-Small
Published
2021-10-30
Public version status
Update
Distribution status
Not 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
LZCPatient Examination Glove, Specialty

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LZAPolymer Patient Examination GloveGeneral Hospital1
LZCMedical Glove, SpecialtyGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20810084210196PackageGS110Not in Commercial Distribution
10810084210199PrimaryGS10
00810084210192Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2081008421019620810084210196
1081008421019910810084210199
00810084210192008100842101928100842101920810084210192

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.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store in cool, dry, and well ventilated space out of direct sunlight.

Regulatory Flags#

DUNS number
815240958
Device count
200
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10810084210007VIVIT8440FW2022-10-28
10810084210014VIVIT10112EM2021-10-30
10810084210021VIVIT8441FW2022-10-28
10810084210038VIVIT10111EM2021-10-30
10810084210045VIVIT30114EM2021-10-30
10810084210052VIVIT31314EM2021-10-30
10810084210069VIVIT313141EMV2021-10-30
10810084210076VIVIT10311TM2021-10-30
10810084210083VIVIT10215TM2021-10-30
10810084210090VIVIT30215TM2021-10-30
10810084210106VIVIT10333TM2021-10-30
10810084210113VIVIT11311TM2021-10-30
10810084210120VIVIT13313TM2021-10-30
10810084210137VIVIT12313TM2021-10-30
10810084210144VIVIT11215TM2021-10-30
10810084210151VIVIT30314TM2021-10-30
10810084210168VIVIT31314TM2021-10-30
10810084210175VIVIT313241TMV2021-10-30
10810084210182VIVIT313242TMV2021-10-30
10810084210205VIVIT205222021-10-30

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Primary DI, Brand, Company table
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09001570557919Sempermed Syntegra preCisionHarps USA, Inc.LZC2026-05-21
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