Primary Device ID | 07340153710139 |
NIH Device Record Key | 801310c7-e658-446e-84e3-e58585960cdb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GETINGE 91-SERIES |
Version Model Number | 9122 |
Catalog Number | 9122-002K960 |
Company DUNS | 354023236 |
Company Name | Getinge Disinfection AB |
Device Count | 1 |
DM Exempt | true |
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 |