Primary Device ID | 16974737271013 |
NIH Device Record Key | c0649485-ed41-4bef-980c-2781d01b4333 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EMSS |
Version Model Number | ET-001 |
Company DUNS | 529436952 |
Company Name | SHANGHAI EMSS MED&TECH 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 | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 06974737271016 [Primary] |
GS1 | 16974737271013 [Package] Contains: 06974737271016 Package: [8 Units] Discontinued: 2023-07-19 Not in Commercial Distribution |
MRI | Orthosis, Truncal/Orthosis, Limb |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-27 |
Device Publish Date | 2023-07-19 |
06974737270064 | EG-006 |
06974737278015 | EH-001 |
16974737271013 | ET-001 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EMSS 86179554 not registered Dead/Abandoned |
IRISS, Inc. 2014-01-30 |
EMSS 78536935 3265830 Dead/Cancelled |
EMSS Holdings (Pty) Ltd. 2004-12-22 |
EMSS 76000451 not registered Dead/Abandoned |
Van de Kop, Franz 2000-03-15 |
EMSS 74251836 1768910 Dead/Cancelled |
W.S.A., Inc. 1992-03-03 |