Primary Device ID | 04053275000011 |
NIH Device Record Key | cededde4-cb5b-4c3b-b627-262c7b364264 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GETINGE |
Version Model Number | 6710 |
Catalog Number | GSS67N Model 6710 |
Company DUNS | 315435859 |
Company Name | MAQUET GmbH |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04053275000011 [Primary] |
FLE | Sterilizer, Steam |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-06 |
04053275000035 | 6717 |
04053275000028 | 6713 |
04053275000011 | 6710 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GETINGE 87358238 5877026 Live/Registered |
Getinge AB 2017-03-03 |
GETINGE 87358210 5877025 Live/Registered |
Getinge AB 2017-03-03 |
GETINGE 77062292 not registered Dead/Abandoned |
Getinge Industrier AB 2006-12-12 |
GETINGE 74512630 1942108 Dead/Cancelled |
GETINGE INDUSTRIER AB 1994-04-14 |
GETINGE 73506524 1384149 Dead/Cancelled |
GETINGE INTERNATIONAL INC. 1984-10-31 |