Primary Device ID | 36945630113629 |
NIH Device Record Key | e0f2b80d-61bd-4916-b274-a68da90f60bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | neoheel |
Version Model Number | 1063T |
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 | 06945630113628 [Unit of Use] |
GS1 | 16945630113625 [Primary] |
GS1 | 36945630113629 [Package] Contains: 16945630113625 Package: carton [4 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 | 2023-05-17 |
Device Publish Date | 2023-05-09 |
36945630113629 | 1063T |
36945630113612 | 1061P |
36945630113605 | 1060M |
36945630113599 | 1062N |
36945630124106 | 1063T |
06945630121821 | 1060M |
36945630121815 | 1062N |
36945630121808 | 1061P |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEOHEEL 87024565 5443944 Live/Registered |
Smiths Medical ASD, Inc. 2016-05-04 |