FDA.reportPublic FDA data

NitraPro

Primary DI
00898110000900
Brand
NitraPro
Company
Medgluv Inc.
Model
MG50161
Catalog number
MG50161
Device description
NitraPro Nitrile Exam Glove, 16in XC, Small
Published
2023-10-31
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

Contact Domains#

Product Codes#

Code, Name table
CodeName
LZCMedical Glove, Specialty

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LZCMedical Glove, SpecialtyGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00898110000900PackageGS110In Commercial Distribution
00898110000818PrimaryGS10
00810145950654Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00898110000900008981100009008981100009000898110000900
00898110000818008981100008188981100008180898110000818
00810145950654008101459506548101459506540810145950654

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

Contacts#

Phone, Email table
PhoneEmail
+1(866)633-4588sales@medgluv.com

Regulatory Flags#

DUNS number
015809044
Device count
50
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
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
00850005229001NitraSoftMG5250MG52502023-10-31
00850005229018NitraSoftMG5251MG52512023-10-31
00850005229025NitraSoftMG5252MG52522023-10-31
00850005229032NitraSoftMG5253MG52532023-10-31
00850005229049NitraSoftMG5254MG52542023-10-31
00850005229056NitraSoftMG5255MG52552023-10-31
00850005229124NitraGrip 300MG5400MG54002023-10-31
00850005229131NitraGrip 300MG5401MG54012023-10-31
00850005229148NitraGrip 300MG5402MG54022023-10-31
00850005229155NitraGrip 300MG5403MG54032023-10-31
00850005229162NitraGrip 300MG5404MG54042023-10-31
00850005229223NitraPlusMG5450MG54502023-10-31
00850005229254NitraPlusMG5453MG54532023-10-31
00850005229261NitraPlusMG5451MG54512023-10-31
00850005229278OysterSkinMG5304MG53042023-10-31
00850005229308Black CobraMG59200MG592002023-10-31
00850005229360NitraPlusMG5452MG54522023-10-31
00850005229483AmethystMG5801MG58012023-10-31
00850005229490AmethystMG5802MG58022023-10-31
00850005229506AmethystMG5803MG58032023-10-31

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Primary DI, Brand, Company table
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