IP Products

Primary DI
00860009119888
Brand
IP Products
Company
IP Products
Model
IPNGB-701
Catalog number
IPNGB-701
Device description
Glove PF Nitrile Exam Blue Small 10/100
Published
2023-02-08
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
LZAPolymer Patient Examination Glove

Product Code Classifications#

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K112294000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K112294000

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00860009119840PackageGS110In Commercial Distribution
00860009119802PrimaryGS10
00860009119888Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00860009119840008600091198408600091198400860009119840
00860009119802008600091198028600091198020860009119802
00860009119888008600091198888600091198880860009119888

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.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
151890902
Device count
100
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00860010093740IP ProductsIPNGK-805IPNGK-8052023-06-19
00860009907621IP ProductsIPNGK-801 IPNGK-801 2023-03-20
00860009907638IP ProductsIPNGK-802IPNGK-802 2023-03-20
00860009907645IP ProductsIPNGK-803IPNGK-8032023-03-20
00860009907652IP ProductsIPNGK-804IPNGK-8042023-03-20
00860009907669IP ProductsIPNGK-801 IPNGK-801 2023-03-20
00860010093719IP ProductsIPNGK-802IPNGK-802 2023-03-20
00860010093726IP ProductsIPNGK-803IPNGK-8032023-03-20
00860010093733IP ProductsIPNGK-804IPNGK-8042023-03-20
00860009119802IP ProductsIPNGB-701IPNGB-7012023-02-08
00860009119819IP ProductsIPNGB-702IPNGB-7022023-02-08
00860009119826IP ProductsIPNGB-703IPNGB-7032023-02-08
00860009119833IP ProductsIPNGB-704IPNGB-7042023-02-08

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Primary DI, Brand, Company table
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