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 |