| Primary Device ID | 10385640064924 |
| NIH Device Record Key | ae32440c-dcad-4f2f-8733-b4dc9524a99e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SUMMIT MEDICAL |
| Version Model Number | AFTD-Y |
| Company DUNS | 965484699 |
| Company Name | SUMMIT MEDICAL, INC. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | 00385640064927 [Primary] |
| GS1 | 00859898006065 [Previous] |
| GS1 | 10385640064924 [Package] Contains: 00385640064927 Package: BOX [10 Units] In Commercial Distribution |
| BYY | Tube, Aspirating, Flexible, Connecting |
| KGZ | Accessories, Catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-05-04 |
| Device Publish Date | 2021-04-26 |
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 |