| Primary Device ID | 10385640063446 |
| NIH Device Record Key | 6139efb8-70bc-470d-8713-60b843720cf0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SUMMIT MEDICAL |
| Version Model Number | 2-90-915 |
| 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 | 00385640063449 [Primary] |
| GS1 | 10385640063446 [Package] Contains: 00385640063449 Package: BOX [250 Units] In Commercial Distribution |
| HOZ | Sponge, Ophthalmic |
| 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 | 2021-01-27 |
| Device Publish Date | 2021-01-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SUMMIT MEDICAL 76311856 3043090 Live/Registered |
SUMMIT MEDICAL LIMITED 2001-09-12 |
![]() SUMMIT MEDICAL 74676630 2038183 Dead/Cancelled |
Summit Medical Systems, Inc. 1995-05-16 |