SEQUENT MR004C
GUDID 20845854036584
SEQUENT MENISCAL REPAIR DEVICE, CURVED NEEDLE, 4 IMPLANTS
Conmed Corporation
Suturing unit, single-use| Primary Device ID | 20845854036584 |
| NIH Device Record Key | 505a465b-4aab-48b3-bca3-2424e4807dc6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SEQUENT |
| Version Model Number | MR004C |
| Catalog Number | MR004C |
| Company DUNS | 071595540 |
| Company Name | Conmed 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 | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854036587 [Package] Package: Box [1 Units] In Commercial Distribution |
| GS1 | 20845854036584 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K102339
FDA Product Code
| MBI | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-02-06 |
| Device Publish Date | 2015-10-24 |
On-Brand Devices [SEQUENT]
| 20845854036584 | SEQUENT MENISCAL REPAIR DEVICE, CURVED NEEDLE, 4 IMPLANTS |
| 20845854036577 | SEQUENT MENISCAL REPAIR DEVICE, CURVED NEEDLE, 3 IMPLANTS |
| 20845854015466 | SEQUENT MENISCAL REPAIR DEVICE, CURVED NEEDLE, 7 IMPLANTS |
| 10845854040416 | SEQUENT DISPOSABLE KIT |
| 20845854031619 | SEQUENT DISPOSABLE SUTURE CUTTER |
Trademark Results [SEQUENT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SEQUENT 87834482 5731289 Live/Registered |
Sequent AG 2018-03-14 |
 SEQUENT 85006366 4339072 Live/Registered |
CONMED CORPORATION 2010-04-05 |
 SEQUENT 79328942 not registered Live/Pending |
AJPM Consulting Pty Ltd 2021-11-26 |
 SEQUENT 79304133 not registered Live/Pending |
SEQUENT AG (SEQUENT SA) (SEQUENT Ltd.) 2020-12-21 |
 SEQUENT 79277665 not registered Live/Pending |
Mandala Förvaltning AB 2019-10-24 |
 SEQUENT 78902798 3459624 Live/Registered |
Sequent Medical, Inc. 2006-06-07 |
 SEQUENT 78341631 3136532 Dead/Cancelled |
Novus International, Inc. 2003-12-16 |
 SEQUENT 78132230 not registered Dead/Abandoned |
Sequent Technologies, Inc. 2002-05-30 |
 SEQUENT 76437869 2977028 Live/Registered |
SOUTHERN COMPANY GAS 2002-08-05 |
 SEQUENT 76409131 2765449 Live/Registered |
SEQUENT, INC. 2002-05-16 |
 SEQUENT 75208061 2119746 Dead/Cancelled |
INTERNATIONAL BUSINESS MACHINES CORP. 1996-12-04 |
 SEQUENT 74626307 2032770 Dead/Cancelled |
INTERNATIONAL BUSINESS MACHINES CORPORATION 1995-01-27 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.