Primary Device ID | 00370858000355 |
NIH Device Record Key | ed26bd67-4c10-4a8f-a9b0-f7afcb8ded88 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BlastX |
Version Model Number | WG-0003 |
Company DUNS | 043989331 |
Company Name | NEXT SCIENCE, LLC |
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 | true |
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 | 00370858000355 [Primary] |
FRO | Dressing, Wound, 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 | 2025-04-22 |
Device Publish Date | 2025-04-14 |
00370858000355 - BlastX | 2025-04-22 |
00370858000355 - BlastX | 2025-04-22 |
00370858000010 - BIOWASH Surgical Irrigation | 2024-08-08 |
00370858000058 - BIOWASH Surgical Irrigation | 2024-08-08 |
00370858000164 - TridentX | 2022-06-09 |
00370858000270 - SITEGUARD | 2022-03-09 |
00370858000218 - XPERIENCE | 2021-05-06 |
00370858000140 - XPERIENCE | 2021-05-06 |
00864076000292 - Bactisure™ | 2020-12-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BLASTX 98326715 not registered Live/Pending |
Blast Analytics & Marketing, Inc. 2023-12-21 |
![]() BLASTX 88375861 5880019 Live/Registered |
Next Science IP Holdings Pty Ltd 2019-04-08 |