Primary Device ID | 08718734963011 |
NIH Device Record Key | bede0c41-f176-4544-91e2-d97b298f416d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CueSee® BGEM |
Version Model Number | 3 |
Catalog Number | 344.003.005 |
Company DUNS | 412925992 |
Company Name | Eurotrol B.V. |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | 08718734962960 [Primary] |
GS1 | 08718734963011 [Package] Contains: 08718734962960 Package: [5 Units] In Commercial Distribution |
OHQ | Multi-Analyte Controls Unassayed |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-04 |
Device Publish Date | 2025-07-25 |
08718734963028 | CueSee® BGEM is an unassayed quality control material intended to verify the precision of pH, p |
08718734963011 | CueSee® BGEM is an unassayed quality control material intended to verify the precision of pH, p |
08718734963004 | CueSee® BGEM is an unassayed quality control material intended to verify the precision of pH, p |
08718734962991 | CueSee® BGEM is an unassayed quality control material intended to verify the precision of pH, p |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CUESEE 85383463 4207468 Live/Registered |
Eurotrol B.V. 2011-07-28 |
![]() CUESEE 79354385 not registered Live/Pending |
Eurotrol B.V. 2022-04-25 |
![]() CUESEE 78678548 3235113 Live/Registered |
EUROTROL B. V. 2005-07-26 |