Primary Device ID | 26945630125120 |
NIH Device Record Key | 440fae1b-bb98-457e-9115-764dc4431393 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Disposable Safety Lancet Press2 |
Version Model Number | 05-062618 |
Company DUNS | 554434897 |
Company Name | Sterilance Medical (Suzhou) Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06945630125126 [Primary] |
GS1 | 26945630125120 [Package] Contains: 06945630125126 Package: [100 Units] In Commercial Distribution |
GS1 | 36945630125127 [Package] Package: [10 Units] In Commercial Distribution |
FMK | Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-08 |
Device Publish Date | 2024-03-31 |