Primary Device ID | 10843152103024 |
NIH Device Record Key | 4509a753-5f27-4739-b889-57ec0bea6aa0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IOPS® |
Version Model Number | T02111 |
Catalog Number | T02111 |
Company DUNS | 080088507 |
Company Name | CENTERLINE BIOMEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
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 | 00843152103027 [Primary] |
GS1 | 10843152103024 [Package] Contains: 00843152103027 Package: Box [5 Units] In Commercial Distribution |
DQK | Computer, Diagnostic, Programmable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-26 |
Device Publish Date | 2025-03-18 |
10843152102058 | Guidewire Handle |
10843152103024 | IOPS Fiducial Tracking Pad is a sterile, single use tracking pad intended for use with the Intra |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() IOPS 90792256 not registered Live/Pending |
CENTERLINE BIIOMEDICAL, INC. 2021-06-24 |
![]() IOPS 90576268 not registered Live/Pending |
The Integration Group of Americas Inc. 2021-03-12 |
![]() IOPS 90290764 not registered Live/Pending |
K1 Investment Management, LLC 2020-10-30 |
![]() IOPS 88331764 not registered Live/Pending |
CENTERLINE BIOMEDICAL, INC. 2019-03-08 |
![]() IOPS 87271055 5425403 Live/Registered |
John Bean Technologies Corporation 2016-12-16 |
![]() IOPS 74065026 1670621 Dead/Cancelled |
Policy Management Systems Corporation 1990-06-04 |