Primary Device ID | 36945630123055 |
NIH Device Record Key | 6b0ab303-8a31-4350-8aec-b7d935cbc1c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterilance Soft Lancet 28G |
Version Model Number | 01-0128 |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06945630123054 [Unit of Use] |
GS1 | 16945630123051 [Primary] |
GS1 | 36945630123055 [Package] Contains: 16945630123051 Package: [50 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 | 2024-01-22 |
Device Publish Date | 2024-01-14 |
26945630125779 - PRESS DISPOSABLE SAFETY LANCET | 2024-05-09 |
36945630125752 - EXALANCE LDE4 Lancing Device | 2024-05-02 |
06945630125522 - STERiLANCE SteriHeel Plus Heel Incision Safety Lancet | 2024-04-17 |
26945630125120 - Disposable Safety Lancet Press2 | 2024-04-08 |
36945630121808 - neoheel | 2024-02-16 |
36945630121815 - neoheel | 2024-02-16 |
06945630121821 - neoheel | 2024-02-16 |
36945630124106 - neoheel | 2024-02-16 |