ClearPort™ Paracentesis Angled 88-2010G
GUDID 10848782023520
ClearPort™ Paracentesis Angled
Surgical Specialties México, S. de R.L. de C.V.
Ophthalmic knife, single-use| Primary Device ID | 10848782023520 |
| NIH Device Record Key | a8aaf9e4-22cd-464d-bb10-3f716ad3346d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ClearPort™ Paracentesis Angled |
| Version Model Number | 88-2010G |
| Catalog Number | 88-2010G |
| Company DUNS | 812762226 |
| Company Name | Surgical Specialties México, S. de R.L. de C.V. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| 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 |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00848782023523 [Primary] |
| GS1 | 10848782023520 [Package] Contains: 00848782023523 Package: Box [5 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K822112
FDA Product Code
| HNN | Knife, ophthalmic |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-07 |
| Device Publish Date | 2020-01-30 |
Devices Manufactured by Surgical Specialties México, S. de R.L. de C.V.
| 20705031227634 - Stratafix Spiral | 2023-12-25 PS-2 2-0 MONODERM 60CM |
| 20705031227986 - Stratafix Spiral | 2023-12-25 PS-2 3-0 MONODERM 30CM |
| 20705031227993 - Stratafix Spiral | 2023-12-25 CT-1 0 MONODERM 45CM |
| 20705031228006 - Stratafix Spiral | 2023-12-25 PS-2 3-0 MONODERM 60CM |
| 20705031228013 - Stratafix Spiral | 2023-12-25 PS-2 2-0 MONODERM 30CM |
| 20705031228020 - Stratafix Spiral | 2023-12-25 CT-1 1 MONODERM 45CM |
| 20705031228037 - Stratafix Spiral | 2023-12-25 SH 0 MONODERM 20CM |
| 20705031228044 - Stratafix Spiral | 2023-12-25 PS-1 2-0 MONODERM 30CM |
Trademark Results [ClearPort]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CLEARPORT 85215874 4009411 Dead/Cancelled |
Scott, Aaron 2011-01-12 |
CLEARPORT 85215874 4009411 Dead/Cancelled |
Terry, Markee 2011-01-12 |
 CLEARPORT 78685429 not registered Dead/Abandoned |
Carter, Shawn 2005-08-04 |
 CLEARPORT 78666767 not registered Dead/Abandoned |
Carter, Shawn 2005-07-08 |
 CLEARPORT 78286780 2964393 Live/Registered |
Surgical Specialties Corporation 2003-08-13 |
 CLEARPORT 78022539 not registered Dead/Abandoned |
Thurman, Roger, Gibson 2000-08-23 |
 CLEARPORT 77196819 3388102 Live/Registered |
CHICAGO MERCANTILE EXCHANGE INC. 2007-06-04 |
 CLEARPORT 75766041 not registered Dead/Abandoned |
KMC Telecom Inc. 1999-08-02 |
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