Embrace Safety Lancet

GUDID 00894030002673

Embrace Safety Lancet 23G/1.8mm 100ct.

OMNIS HEALTH, LLC

Blood lancet, single-use
Primary Device ID00894030002673
NIH Device Record Key96e23587-bb3d-4b55-b139-d5399adc8876
Commercial Distribution StatusIn Commercial Distribution
Brand NameEmbrace Safety Lancet
Version Model NumberSHN02GX23.18
Company DUNS824763358
Company NameOMNIS HEALTH, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter
Needle Gauge23 Gauge
Length1.8 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100894030002673 [Primary]

FDA Product Code

FMKLancet, Blood

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-13
Device Publish Date2021-07-05

On-Brand Devices [Embrace Safety Lancet]

00894030002673Embrace Safety Lancet 23G/1.8mm 100ct.
00894030002659Embrace Safety Lancet 30G/1.8mm 100ct.
00894030002512Embrace Safety Lancet 21G/2.2mm 100ct.

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