Primary Device ID | 00854204008597 |
NIH Device Record Key | bb3959e0-4135-48c2-b009-0c5861fa31d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Setmark Inc. |
Version Model Number | NF300/627710 |
Company DUNS | 080798558 |
Company Name | SETMARK INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |