Primary Device ID | 00816711023487 |
NIH Device Record Key | 7439f030-581b-4a07-a069-4c39b6ded115 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | O2 HOSE, DISS F X DISS F |
Version Model Number | 92305110-4 |
Catalog Number | 92305110-4 |
Company DUNS | 004175550 |
Company Name | PARKER-HANNIFIN CORPORATION |
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 | 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 | true |
OTC Over-The-Counter | false |