Primary Device ID | 35019517065965 |
NIH Device Record Key | 8f5a16f5-12ad-43de-8526-f82ef62ce2ab |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EchoGlo |
Version Model Number | 24-4101-24 |
Company DUNS | 106712748 |
Company Name | SMITHS MEDICAL MD, 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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15019517065961 [Primary] |
GS1 | 35019517065965 [Package] Contains: 15019517065961 Package: BOX [25 Units] In Commercial Distribution |
GS1 | 55019517065969 [Package] Package: CARTON [16 Units] In Commercial Distribution |
BSP | NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-17 |
Device Publish Date | 2018-03-19 |
35019517086953 | 24-4121-24 |
35019517086946 | 24-4120-24 |
55019517086933 | 24-4119-24 |
35019517086922 | 24-4118-24 |
55019517086919 | 24-4117-24 |
35019517086908 | 24-4116-24 |
55019517086896 | 24-4115-24 |
35019517086885 | 24-4114-24 |
55019517066003 | 24-4105-24 |
55019517065990 | 24-4104-24 |
55019517065983 | 24-4103-24 |
35019517065972 | 24-4102-24 |
35019517065965 | 24-4101-24 |
55019517065952 | 24-4100-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ECHOGLO 87686953 not registered Live/Pending |
Smiths Medical ASD, Inc. 2017-11-16 |
![]() ECHOGLO 85752562 4373747 Live/Registered |
Smiths Medical ASD, Inc. 2012-10-12 |