Primary Device ID | 00369771000832 |
NIH Device Record Key | d364c0d3-2570-43b2-b104-6345bcbcf9b4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Syringes Safety |
Version Model Number | 11466 |
Company DUNS | 361663839 |
Company Name | GERI-GENTLE CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |