Primary Device ID | 00816711024934 |
NIH Device Record Key | 6ebf5430-fb2a-437d-9056-43bbb99e30cf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HA,O2,INTL (DISSF X DISSF)2FT |
Version Model Number | 92305297-2 |
Catalog Number | 92305297-2 |
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 |
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