Primary Device ID | 00840165500034 |
NIH Device Record Key | f75e7d80-1ec5-41db-aa54-96611f118947 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Leakbuster |
Version Model Number | B1202-1O |
Company DUNS | 859771235 |
Company Name | Starplex Scientific Corp. |
Device Count | 75 |
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 | 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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840165500027 [Unit of Use] |
GS1 | 00840165500034 [Package] Contains: 10840165500024 Package: [4 Units] In Commercial Distribution |
GS1 | 10840165500024 [Primary] |
FMH | Container, Specimen, Sterile |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-25 |
Device Publish Date | 2025-03-17 |
00840165500034 | Specimen Container, 120 ml, Orange Cap, Sterile. |
00840165500010 | Specimen Container, 90 ml, Orange Cap, Sterile. |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() LEAKBUSTER 78787567 not registered Dead/Abandoned |
Greene, Tweed of Delaware, Inc. 2006-01-09 |
![]() LEAKBUSTER 76362892 not registered Dead/Abandoned |
Greene, Tweed of Delaware, Inc. 2002-01-25 |
![]() LEAKBUSTER 74409307 1906530 Dead/Cancelled |
Greene, Tweed of Delaware, Inc. 1993-07-01 |