Primary Device ID | 07340153700161 |
NIH Device Record Key | 35baa7db-34ef-49c4-baf7-296ed5dc143b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GETINGE 91-SERIES |
Version Model Number | 9128 |
Catalog Number | 9128-002 |
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 | true |
Manufacturing Date | true |
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 |