| Primary Device ID | 07613327137392 |
| NIH Device Record Key | a67c5d41-3248-410e-94e2-2d8683b4def8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProCinch |
| Version Model Number | 234-102-090 |
| Catalog Number | 234-102-090 |
| Company DUNS | 187502109 |
| Company Name | STRYKER 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
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| Phone | +1(866)624-4422 |
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| Phone | +1(866)624-4422 |
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| Phone | +1(866)624-4422 |
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| Phone | +1(866)624-4422 |
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| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
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| Phone | +1(866)624-4422 |
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| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327137392 [Primary] |
| HTY | PIN, FIXATION, SMOOTH |
| MBI | Fastener, fixation, nondegradable, soft tissue |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-14 |
| 07613327137392 | PROCINCH ADJUSTABLE LOOP IMPLANT, STANDARD TENSIONING |
| 07613327137385 | PROCINCH ADJUSTABLE LOOP IMPLANT, REVERSE TENSIONING |
| 07613327543117 | PROCINCH NO BUTTON ADJUSTABLE LOOP IMPLANT |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PROCINCH 87433182 not registered Dead/Abandoned |
FIDELITY INFORMATION SERVICES, LLC 2017-05-02 |
![]() PROCINCH 86436802 4890371 Live/Registered |
Stryker Corporation 2014-10-28 |