ENCORE

Primary DI
20884792209520
Brand
ENCORE
Company
Ansell
Model
5795002
Catalog number
5795002
Device description
ENCORE® Latex Acclaim Size 6.5, Sterile Latex Powder-Free Surgical Glove
Published
2021-07-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
KGOSurgeon'S Gloves
LZCPatient Examination Glove, Specialty

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KGOSurgeon'S GlovesGeneral, Plastic Surgery1
LZCMedical Glove, SpecialtyGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20884792209520PackageGS150In Commercial Distribution
30884792209527PackageGS14In Commercial Distribution
00884792209526PrimaryGS10
00071483000023Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2088479220952020884792209520
3088479220952730884792209527
00884792209526008847922095268847922095260884792209526
00071483000023000714830000230714830000230071483000023

GMDN Terms#

Term, Definition table
TermDefinition
Hevea-latex surgical glove, non-powdered, non-antimicrobialA device made of Hevea natural rubber latex (NRL) intended as a protective barrier when worn on the hands of healthcare providers at the surgical site; 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 both the patient and the staff against contamination from microorganisms. It will have appropriate characteristics regarding tactility/comfort of use, and should provide appropriate physical properties (e.g., strength, elasticity), and uniformity of dimensions. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
775-746-6600jacob.ramirez@ansell.com

Regulatory Flags#

DUNS number
120522524
Device count
2
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
true
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00076490718282HALYARDSGL85055BSGL85055B2024-07-19
00076490718299HALYARDSGL85060BSGL85060B2024-07-19
00076490718305HALYARDSGL85065BSGL85065B2024-07-19
00076490718312HALYARDSGL85070BSGL85070B2024-07-19
00076490718329HALYARDSGL85075BSGL85075B2024-07-19
00076490718336HALYARD SGL85080BSGL85080B2024-07-19
00076490718343HALYARDSGL85085BSGL85085B2024-07-19
00076490718350HALYARDSGL85090BSGL85090B2024-07-19
10076490705654HALYARDSGL85055BSGL85055B2024-07-19
10076490705661HALYARDSGL85060BSGL85060B2024-07-19
10076490705678HALYARDSGL85065BSGL85065B2024-07-19
10076490705685HALYARDSGL85070BSGL85070B2024-07-19
10076490705692HALYARDSGL85075BSGL85075B2024-07-19
10076490705708HALYARD SGL85080BSGL85080B2024-07-19
10076490705715HALYARDSGL85085BSGL85085B2024-07-19
10076490705722HALYARDSGL85090BSGL85090B2024-07-19
10680651190557HALYARDSGL99055SGL990552024-07-12
10680651190601HALYARDSGL99060SGL990602024-07-12
10680651190656HALYARDSGL99065SGL990652024-07-12
10680651190700HALYARDSGL99070SGL990702024-07-12

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