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 |