FDA.reportPublic FDA data

Home Green Leaf

Primary DI
00608106001015
Brand
Home Green Leaf
Company
UNIWARE HOUSEWARE CORP.
Model
C2046M-NLD
Device description
4.6gram medical exam glove
Published
2019-10-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
QDOFentanyl And Other Opioid Protection Glove

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
QDOFentanyl And Other Opioid Protection GloveGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00608106001015PackageGS110In Commercial Distribution
00608106000988PrimaryGS10
00608106000995Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00608106001015006081060010156081060010150608106001015
00608106000988006081060009886081060009880608106000988
00608106000995006081060009956081060009950608106000995

GMDN Terms#

Term, Definition table
TermDefinition
Nitrile examination/treatment glove, non-powdered, non-sterileA non-sterile 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.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
931896372
Device count
100
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 DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00608106000070Home Green LeafC2037L2019-06-17
00608106000179Home Green LeafC2037M2019-06-17
00608106000230Home Green LeafC2037S2019-06-17
00608106000377Home Green LeafC2037XL2019-06-17
00608106000469Home Green LeafC2046L2019-06-17
00608106000490Home Green LeafC2046M2019-06-17
00608106000520Home Green LeafC2046S2019-06-17
00608106000568Home Green LeafC2046XL2019-06-17
00608106001206Home Green LeafC2060S2023-06-01
00608106001244Home Green LeafC2060M2023-06-01
00608106001282Home Green LeafC2060L2023-06-01
00608106001343Home Green LeafC2060XL2023-06-01
00608106001367Home Green LeafC2160S2023-06-01
00608106001381Home Green LeafC2160M2023-06-01
00608106001411Home Green LeafC2160L2023-06-01
00608106001435Home Green LeafC2160XL2023-06-01
00608106001213Home Green LeafC2060S2023-06-01
00608106001268Home Green LeafC2060M2023-06-01
00608106001299Home Green LeafC2060L2023-06-01
00608106001350Home Green LeafC2060XL2023-06-01

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Primary DI, Brand, Company table
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20680651500704HalyardO&M HALYARD, INC.QDO2026-06-04
20680651500711HalyardO&M HALYARD, INC.QDO2026-06-04
20680651502388HalyardO&M HALYARD, INC.QDO2026-06-04
20680651502395HalyardO&M HALYARD, INC.QDO2026-06-04
20680651502401HalyardO&M HALYARD, INC.QDO2026-06-04
20680651502418HalyardO&M HALYARD, INC.QDO2026-06-04
20680651502425HalyardO&M HALYARD, INC.QDO2026-06-04
10810141933740VIVIT SupplyVivit Supply LLCQDO2026-02-03
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10810141933771VIVIT SupplyVivit Supply LLCQDO2026-02-03
10810141933788VIVIT SupplyVivit Supply LLCQDO2026-02-03
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