Primary Device ID | 06945630109133 |
NIH Device Record Key | f17a3290-d005-480f-b088-12ca8e9dfc48 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sterilance Press2 Pressure Activated Safety Lancet |
Version Model Number | 05-062618 |
Company DUNS | 421141183 |
Company Name | SteriLance Medical (Suzhou) Inc. |
Device Count | 50 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
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 | true |