Primary Device ID | 06970283131002 |
NIH Device Record Key | f5cf4694-00a3-422b-ab04-521b40be02b6 |
Commercial Distribution Discontinuation | 2099-12-31 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MODUEVO |
Version Model Number | ENERGY |
Company DUNS | 545372336 |
Company Name | Maquet (Suzhou) Co. LTD |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06970283131002 [Primary] |
BYX | Tubing, Pressure And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-15 |
Device Publish Date | 2022-12-07 |
06970283131026 | Medical Ceiling Supply Units |
06970283131019 | Medical Ceiling Supply Units |
06970283131002 | Medical Ceiling Supply Units |
06970283130999 | Medical Ceiling Supply Units |
06970283130982 | Medical Ceiling Supply Units |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MODUEVO 87019085 5381410 Live/Registered |
Maquet(Suzhou)Co., Ltd. 2016-04-29 |