Primary Device ID | 20369771000898 |
NIH Device Record Key | 1ffd79dc-043f-4d81-8d35-f4004e24b1e7 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |