Primary Device ID | 00860004575634 |
NIH Device Record Key | 743a3163-eced-4e54-89f6-ef366ffe241f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Assembly Required Distributors Inc. |
Version Model Number | AR2204X-01-22 |
Company DUNS | 170562396 |
Company Name | ASSEMBLY REQUIRED DISTRIBUTORS 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 | 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 |