Primary Device ID | 00854362008545 |
NIH Device Record Key | baca4b57-ab8e-410f-857f-2a0d59a10f2b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Assembly Required Distributors Inc. |
Version Model Number | 0000-233 |
Company DUNS | 170562396 |
Company Name | Assembly Required Distributors Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
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 |