INSTRUSAFE
GUDID 00385640052191
SUMMIT MEDICAL, INC.
Instrument tray| Primary Device ID | 00385640052191 |
| NIH Device Record Key | 1fe37a22-acef-46e4-bfda-e65c71a9d16f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | INSTRUSAFE |
| Version Model Number | IN-2020-2345 |
| 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 | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00385640052191 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K051157
FDA Product Code
| KCT | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-13 |
| Device Publish Date | 2020-05-05 |
On-Brand Devices [INSTRUSAFE]
Trademark Results [INSTRUSAFE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INSTRUSAFE 85717324 4309161 Live/Registered |
Summit Medical, Inc. 2012-08-30 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.