| Primary Device ID | 00733132644575 |
| NIH Device Record Key | e4da705f-7648-453b-81b5-556a4aaba510 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GORE ENFORM Preperitoneal Biomaterial |
| Version Model Number | GBWR1010 |
| Catalog Number | GBWR1010 |
| Company DUNS | 967358115 |
| Company Name | W. L. Gore & Associates, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| 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 |
| Width | 10 Centimeter |
| Width | 10 Centimeter |
| Width | 10 Centimeter |
| Width | 10 Centimeter |
| Length | 10 Centimeter |
| Width | 10 Centimeter |
| Length | 10 Centimeter |
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| Length | 10 Centimeter |
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| Length | 10 Centimeter |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00733132644575 [Primary] |
| OWT | Mesh, Surgical, Absorbable, Abdominal Hernia |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-29 |
| Device Publish Date | 2018-09-28 |
| 00733132644674 | GBWR3040 |
| 00733132644667 | GBWR2540 |
| 00733132644650 | GBWR3030 |
| 00733132644643 | GBWR2040 |
| 00733132644636 | GBWR2030 |
| 00733132644629 | GBWR2025 |
| 00733132644612 | GBWR2020 |
| 00733132644605 | GBWR1620 |
| 00733132644599 | GBWR1016 |
| 00733132644582 | GBWR0816 |
| 00733132644575 | GBWR1010 |
| 00733132644568 | GBWR0616 |