FreeStyle

Primary DI
10810007660360
Brand
FreeStyle
Company
HOURGLASS INTERNATIONAL INC
Model
1103
Device description
Nitrile Powder Free Examination Gloves, L, Tested for Use with Chemotherapy Drugs.
Published
2021-12-01
Public version status
New
Distribution status
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
20810007660367PrimaryGS10
00810007660363Unit of UseGS10
10810007660360Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2081000766036720810007660367
00810007660363008100076603638100076603630810007660363
1081000766036010810007660360

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 under cool dry conditions. Avoid direct sunlight. Open box should be shielded from direct sunlight or fluorescent lighting.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
026777252
Device count
100
Premarket exempt
true
Lot or batch
true
Manufacturing date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810007662336NUSA2002026-01-01
00810007662343NUSA2012026-01-01
00810007662350NUSA2022026-01-01
00810007662367NUSA2032026-01-01
00810007662374NUSA2042026-01-01
00810007662381NUSA2002026-01-01
00810007662398NUSA2012026-01-01
00810007662404NUSA2022026-01-01
00810007662411NUSA2032026-01-01
00810007662428NUSA2042026-01-01
00810007662480HANDPRO55002025-12-15
00810007662497HANDPRO55012025-12-15
00810007662503HANDPRO55022025-12-15
00810007662510HANDPRO55032025-12-15
00810007662527HANDPRO55042025-12-15
00810007662596HANDPRO55052025-12-15
00810007662534HANDPRO55002025-12-15
00810007662541HANDPRO55012025-12-15
00810007662558HANDPRO55022025-12-15
00810007662565HANDPRO55032025-12-15

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