| Primary Device ID | 00385640063739 | 
| NIH Device Record Key | 3e9c9c29-1ba2-4550-b98a-a54e4a4128a0 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | INSTRUSAFE | 
| Version Model Number | IN-2020-4314 | 
| Company DUNS | 965484699 | 
| Company Name | SUMMIT MEDICAL, INC. | 
| 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 | true | 
| Serial Number | false | 
| Manufacturing Date | true | 
| Expiration Date | false | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | true | 
| RX Perscription | false | 
| OTC Over-The-Counter | true | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00385640063739 [Primary] | 
| KCT | Sterilization Wrap Containers, Trays, Cassettes & Other 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 | 2021-02-23 | 
| Device Publish Date | 2021-02-15 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  INSTRUSAFE  85717324  4309161 Live/Registered | Summit Medical, Inc. 2012-08-30 |