Primary Device ID | B718DL82030 |
NIH Device Record Key | d76e1600-8c03-4efd-94c3-326aba2d0c3c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multiplace Hyperbaric Oxygen Treatment Chamber |
Version Model Number | DL8 |
Catalog Number | DL8203 |
Company DUNS | 748668373 |
Company Name | FINK ENGINEERING PTY LTD |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 |