| Primary Device ID | 00850013050185 |
| NIH Device Record Key | 0e78779b-b3af-424d-ba17-77b987c6720f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SureGuide |
| Version Model Number | 4143 |
| Company DUNS | 785275777 |
| Company Name | Clinicon Corporation |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| 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 | 00850013050185 [Primary] |
| GEX | Powered Laser Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
[00850013050185]
Ethylene Oxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-05-14 |
| Device Publish Date | 2021-05-06 |
| 00850013050185 | SureGuide, 2.75m Fiber Cable Assembly, ST Connector |
| 00850013050178 | SureGuide, 2.75m Fiber Cable Assembly,SMA with Interlock Wire |
| 00850013050161 | SureGuide, 2.00m Fiber Cable Assembly, ST Connector |
| 00850013050154 | SureGuide, 2.00m Fiber Cable Assembly, SMA Connector with Interlock Wire |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SUREGUIDE 90408347 not registered Live/Pending |
Spinal Elements, Inc. 2020-12-23 |
![]() SUREGUIDE 88642389 not registered Live/Pending |
Benvenue Medical, Inc. 2019-10-04 |
![]() SUREGUIDE 86299027 4770172 Live/Registered |
Agilent Technologies, Inc. 2014-06-03 |
![]() SUREGUIDE 86231342 4730267 Live/Registered |
IPT Global, LLC 2014-03-25 |
![]() SUREGUIDE 77956888 not registered Dead/Abandoned |
Clinicon Corporation 2010-03-11 |
![]() SUREGUIDE 75701178 not registered Dead/Abandoned |
Hewlett-Packard Company 1999-05-06 |
![]() SUREGUIDE 74443237 1841767 Dead/Cancelled |
St. Jude Medical, Inc., Cardiac Assist Division 1993-10-04 |
![]() SUREGUIDE 74137522 not registered Dead/Abandoned |
St. Jude Medical, Inc., Cardiac Assist Division 1991-02-08 |