Primary Device ID | 00841034112570 |
NIH Device Record Key | de9a525d-b291-4b24-a2f3-f2ef245f8e3d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PATIENT CABLE - 10 LD FX BN |
Version Model Number | KKB003 |
Catalog Number | KKB003 |
Company DUNS | 066232067 |
Company Name | RPI |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 |