FDA.report

MediChoice

Primary DI
50885632136397
Brand
MediChoice
Company
OWENS & MINOR DISTRIBUTION, INC.
Model
GLV2301
Device description
Glove Exam Nitrile Xt Next Generation 9.5-Inch Cuff Small Non-Sterile Ambidextrous Powder-Free Textured Beaded Cuff Disposable Cleared For Use With Some Chemotherapy Drugs Not Made With Natural Rubber Latex MediChoice
Published
2020-09-29
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
LZAPolymer patient examination glove

Product Code Classifications

CodeDeviceSpecialtyClass
LZAPolymer Patient Examination GloveGeneral Hospital1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
50885632136397PackageGS110In Commercial Distribution
30885632136393PrimaryGS10
10885632136399Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalized
5088563213639750885632136397
3088563213639330885632136393
1088563213639910885632136399

GMDN Terms

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

TypeLowHighCondition
Special Storage Condition, Specify00
Special Storage Condition, Specify00Store under cool, dry conditions. Avoid direct sunlight. Open box should be shielded from direct sunlight, fluorescent lighting or other source of ozone.

Sterilization Methods

Method

Regulatory Flags

DUNS number
007941230
Device count
200
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
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

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