Primary Device ID | 07340153710221 |
NIH Device Record Key | 50a6cbf5-e975-46e3-bd9b-a3dfb49c4344 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GETINGE 1800-SERIES |
Version Model Number | FD1810 |
Catalog Number | FD1810-001K906 |
Company DUNS | 354023236 |
Company Name | Getinge Disinfection AB |
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 | false |
OTC Over-The-Counter | false |