| 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 | 
| 06974737270125 | EG-010B3 | 
| 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 |