| Primary Device ID | 90817266020542 | 
| NIH Device Record Key | 6f7be101-d125-435b-8822-42026cdae466 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Patient Cables | 
| Version Model Number | 425XX | 
| Company DUNS | 180587883 | 
| Company Name | MERIT CABLES INCORPORATED | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Unsafe | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | false | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | false | 
| Expiration Date | false | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | true | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Length | 14 Feet | 
| Length | 13 Feet | 
| Length | 14 Feet | 
| Length | 13 Feet | 
| Length | 14 Feet | 
| Length | 13 Feet | 
| Length | 14 Feet | 
| Length | 13 Feet | 
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| Length | 13 Feet | 
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| Length | 14 Feet | 
| Length | 13 Feet | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 90817266020542 [Primary] | 
| DSA | Cable, Transducer And Electrode, Patient, (Including Connector) | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2018-03-29 | 
| Device Publish Date | 2016-09-23 | 
| 90817266020832 | 5 Lead Patient Trunk Cable | 
| 90817266020542 | Patient Cable Non Detachable 5 Lead |