Primary Device ID | 00842209104734 |
NIH Device Record Key | b132b280-01f6-413b-b609-896124b50021 |
Commercial Distribution Discontinuation | 2023-11-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | NAR |
Version Model Number | 85-1576 |
Company DUNS | 832426782 |
Company Name | NORTH AMERICAN RESCUE, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 | false |
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