Primary Device ID | 00840828174770 |
NIH Device Record Key | 5a79aefd-f4c3-48b4-bbb9-215a4f63789d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BA KIT,WE,P1801,DU,1',BE,P37,INL,6',NO T |
Version Model Number | BCC-3018-L01-E06-001 |
Catalog Number | 25601 |
Company DUNS | 796452311 |
Company Name | CURBELL MEDICAL PRODUCTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |