Primary Device ID | 26945630121252 |
NIH Device Record Key | 50b375bf-3248-422b-97a8-798f69620e5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterile Blood Lancet |
Version Model Number | SHN02GM0123-50 |
Company DUNS | 554434897 |
Company Name | Sterilance Medical (Suzhou) Inc. |
Device Count | 50 |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06945630121258 [Unit of Use] |
GS1 | 16945630121255 [Primary] |
GS1 | 26945630121252 [Package] Contains: 16945630121255 Package: [40 Units] In Commercial Distribution |
GS1 | 36945630121259 [Package] Package: [5 Units] In Commercial Distribution |
QRK | Single Use Only Blood Lancet Without 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 | 2023-10-09 |
Device Publish Date | 2023-09-30 |