| Primary Device ID | H6680921328S1 |
| NIH Device Record Key | d839008e-c228-441b-b799-095a0333bc65 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bosworth Aegis |
| Version Model Number | 0921328S |
| Catalog Number | 0921328S |
| Company DUNS | 014769301 |
| Company Name | Harry J Bosworth Company |
| 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(800)333-3131 |
| tschwear@keystoneind.com |
| Total Volume | 0.4 Milliliter |
| Storage Environment Temperature | Between 32 Degrees Fahrenheit and 86 Degrees Fahrenheit |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | H6680921328S1 [Primary] |
| EBC | SEALANT, PIT AND FISSURE, AND CONDITIONER |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-15 |
| H66809213481 | Aegis Pit & Fissure Sealant w/ACP Standard Kit |
| H6680921328S1 | Aegis Pit & Fissure Sealant w/ACP 0.4 mL Sample |
| H66809213281 | Aegis Pit & Fissure Sealant w/ACP Refill Kit |
| H66809213271 | Aegis Pit & Fissure Sealant w/ACP Clinic Kit |