Primary Device ID | 00385640053785 |
NIH Device Record Key | bd27dd43-5bf5-4170-aa9b-c99316570616 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SUMMIT MEDICAL |
Version Model Number | 3-TT-FILTRON 2000 |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00385640053785 [Primary] |
GS1 | 10385640053782 [Package] Package: BOX [1 Units] In Commercial Distribution |
MUU | System, Suction, Lipoplasty |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-08-23 |
Device Publish Date | 2021-04-20 |
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 |