| Primary Device ID | 00821925039698 |
| NIH Device Record Key | 6f2a61e6-8138-48e9-830f-e48e2d3e2adf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ARMSTRONG BEVELED GROMMET PACIFIC 114 MM ID FLUOROPLASTICPC COATED |
| Version Model Number | 70146067 |
| Company DUNS | 007198742 |
| Company Name | Gyrus Acmi, Inc. |
| Device Count | 2 |
| 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 | false |
| OTC Over-The-Counter | false |
| Phone | 18002623540 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00821925021013 [Package] Package: [60 Units] In Commercial Distribution |
| GS1 | 00821925039698 [Primary] |
| GS1 | 00821925040762 [Unit of Use] |
| ETD | Tube, Tympanostomy |
| 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 | 2015-10-24 |
| 00821925039698 | Ventilate the middle ear subsequent to otitis media Elimiate fluid buildup in the middle ear whi |
| 00821925025424 | Ventilate the middle ear subsequent to otitis media Elimiate fluid buildup in the middle ear whi |