Primary Device ID | 36945630132477 |
NIH Device Record Key | 39c03750-3926-4528-b44c-42aeb15eef34 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STERiLANCE Press2 Disposable Safety Lancet |
Version Model Number | 05-062118 |
Company DUNS | 554434897 |
Company Name | Sterilance Medical (Suzhou) Inc. |
Device Count | 100 |
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 | 06945630132476 [Unit of Use] |
GS1 | 16945630132473 [Primary] |
GS1 | 36945630132477 [Package] Contains: 16945630132473 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 | 2024-10-31 |
Device Publish Date | 2024-10-23 |
36945630115081 | 05-063018 |
36945630115074 | 05-062818 |
36945630131081 | 05-063018 |
36945630132408 | 05-062122 |
36945630132392 | 05-062122 |
36945630132507 | 05-063012 |
36945630132491 | 05-062812 |
36945630132484 | 05-062620 |
36945630132477 | 05-062118 |