Primary Device ID | 00841034112242 |
NIH Device Record Key | 4bb54371-b40c-431a-9b29-12e71d7a3fef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PATIENT CABLE - 3 LD FX SN |
Version Model Number | KCB002 |
Catalog Number | KCB002 |
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 |