| Primary Device ID | EYET7600015 |
| NIH Device Record Key | 53522600-0869-4d6a-b4c5-9f7cfe9ee315 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 760-0015 |
| Company DUNS | 324001916 |
| Company Name | Yeti Dentalprodukte GmbH |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EYET7600015 [Primary] |
| EGD | WAX, DENTAL, INTRAORAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-05-22 |
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| EYET3201506 - K2 OPAQUER powder, O-B1, 15g | 2025-05-01 |
| EYET3201507 - K2 OPAQUER powder, O-B2, 15g | 2025-05-01 |
| EYET3201508 - K2 OPAQUER powder, O-B3, 15g. | 2025-05-01 |