Primary Device ID | 09341394009288 |
NIH Device Record Key | 9b9f4e16-469a-4fdb-9572-381db10fbbe0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SUREFILL |
Version Model Number | AK25AW |
Catalog Number | AK25AW |
Company DUNS | 008186174 |
Company Name | AERO HEALTHCARE (US), LLC |
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 | true |
Device Combination Product | true |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09341394009288 [Primary] |
LRR | First Aid Kit With Drug |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-18 |
Device Publish Date | 2023-12-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUREFILL 90609199 not registered Live/Pending |
Aero Health Aust Pty Ltd 2021-03-29 |
SUREFILL 90609197 not registered Live/Pending |
Aero Health Aust Pty Ltd 2021-03-29 |
SUREFILL 88659651 not registered Live/Pending |
Reliable Packaging Systems Inc 2019-10-18 |
SUREFILL 88388165 5868517 Live/Registered |
SCHOLLE IPN CORPORATION 2019-04-16 |
SUREFILL 87079038 5133050 Live/Registered |
Baker Hughes Incorporated 2016-06-21 |
SUREFILL 77023087 3527991 Live/Registered |
FXI, INC. 2006-10-17 |
SUREFILL 75879430 2464652 Live/Registered |
SIEMENS HEALTHCARE DIAGNOSTICS INC. 1999-12-22 |
SUREFILL 75262353 not registered Dead/Abandoned |
Safe Alternatives Corporation of America, Inc. 1997-03-21 |
SUREFILL 74705160 2149632 Dead/Cancelled |
HORSTINE FARMERY LIMITED 1995-07-19 |