Diska Nulife

Primary DI
00810115891734
Brand
Diska Nulife
Company
Diska LLC
Model
I
Device description
Single Use Lancets
Published
2023-08-25
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
QRLMultiple Use Blood Lancet For Single Patient Use Only

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
QRLMultiple Use Blood Lancet For Single Patient Use OnlyGeneral, Plastic Surgery2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810115891734PackageGS1400In Commercial Distribution
00810115891710PrimaryGS10
00810115891727Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810115891734008101158917348101158917340810115891734
00810115891710008101158917108101158917100810115891710
00810115891727008101158917278101158917270810115891727

GMDN Terms#

Term, Definition table
TermDefinition
Glucose monitoring system IVD, home-useA collection of devices including a portable, battery-powered, semi-automated or automated instrument (self-testing meter), reagents, test strips and/or other associated materials and accessories (e.g., control solutions, lancets) intended to be used for the quantitative measurement of glucose in a whole blood clinical specimen; it is designed to be used for self-testing by a layperson in the home, and some types may in addition be used at the point-of-care. Measured glucose values are used to manage blood glucose levels, primarily by persons with diabetes mellitus.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
201-675-6037ashish.bharal@diskatech.com

Regulatory Flags#

DUNS number
006311259
Device count
50
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
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810115891581Diska NulifeDNL-TMB-2282-G2023-08-25
00810115891697Diska NulifeDNL-TTS012023-08-25
00810115892328Diska NulifeDNL-TMB2084-A2023-10-20
00810115892342Diska NuLifeVGM04(Ref. DNL-VGM04)2023-10-05
00810115892427Diska NuLifeVGS01 (REF: DNL-VGS01)2023-10-05
00810115892335Diska NulifeDNL-TMB2084-A2023-10-20
00810115892366Diska NuLifeDNL-GBS-2012-B2023-10-05
00810115892380Diska NuLifeDNL-YM4022023-10-05
00810115892458Diska NuLifeDNL-VGC012023-10-05
00810115892359Diska NuLifeVGM04(Ref. DNL-VGM04)2023-10-05
00810115892373Diska NuLifeDNL-GBS-2012-B2023-10-05
00810115892403Diska NuLifeDNL-YM4022023-10-05
00810115892441Diska NuLifeVGS01 (REF: DNL-VGS01)2023-10-05
00810115892465Diska NuLifeDNL-VGC012023-10-05
00810115891642Diska NulifeHH-XIII-T2023-08-25
00810115891666Diska NulifeTCS012023-08-25
00810115891710Diska NulifeI2023-08-25
00810115891598Diska NulifeDNL-TMB-2282-G2023-08-25
00810115891659Diska NulifeHH-XIII-T2023-08-25
00810115891673Diska NulifeTCS012023-08-25

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Primary DI, Brand, Company table
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00860015383952True IntegralTRUE INTEGRAL INCQRL2026-04-14
16945630142007STERiLANCESterilance Medical (Suzhou) Inc.QRL2026-03-09
36945630142001STERiLANCESterilance Medical (Suzhou) Inc.QRL2026-03-09
00850080988107AUVONUAN HEALTHCARE LIMITEDQRL2026-03-02
00850080988114AUVONUAN HEALTHCARE LIMITEDQRL2026-03-02
00810079240579Teladoc Health, Inc.Teladoc Health, Inc.QRL2026-02-17
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MHC1732101Members MarkMHC MEDICAL PRODUCTS, LLCQRL2025-09-16
06949517009028One +StepShandong Lianfa Medical Plastic Products CO.,LTDQRL2025-09-14
MHC18080020EasyTouchMHC MEDICAL PRODUCTS, LLCQRL2025-08-04
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