| Primary Device ID | 13661522025069 |
| NIH Device Record Key | 73dd58b0-3701-4056-9d78-e46ceba14dea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SINUSORB® PGA |
| Version Model Number | 8142 |
| Company DUNS | 265741780 |
| Company Name | PETERS SURGICAL |
| 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 | 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03661522025062 [Primary] |
| GS1 | 13661522025069 [Package] Contains: 03661522025062 Package: [12 Units] In Commercial Distribution |
| GAM | SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-17 |
| Device Publish Date | 2020-01-09 |
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