Primary Device ID | 04713648766493 |
NIH Device Record Key | 22ddb5fc-5916-4b44-8348-32c95ef89f86 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ApexBio SteriLance BLOOD LANCET (Sterile) |
Version Model Number | lancet |
Company DUNS | 657608092 |
Company Name | APEX BIOTECHNOLOGY CORP. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04713648766493 [Primary] |
FMK | Lancet, Blood |
QRK | Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-25 |
Device Publish Date | 2020-05-15 |
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04713648766493 - ApexBio SteriLance BLOOD LANCET (Sterile) | 2020-05-25 |
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