| Primary Device ID | 00721902720529 |
| NIH Device Record Key | 000e3645-dcaa-4ab8-9a67-09b6c1b828a3 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 1150050 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | false |
| 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)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00721902720529 [Primary] |
| ETA | REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL |
| 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 | 2015-06-09 |
| 20763000888989 - Merocel | 2026-03-16 SPONGE 400515 10PK KENNEDY INTRANASAL |
| 20763000888996 - Merocel | 2026-03-16 PACKING 440412 MEROCEL 10PK DOYLE NASAL |
| 00763000892951 - M4 | 2026-03-09 MICRODEBRIDER 1898200T IGS M4 ROHS |
| 00199150023851 - N/A | 2026-02-24 PROBE 8225101E PRASS STD PROT HANDLE |
| 00199150023868 - N/A | 2026-02-24 PROBE 8225101 5PK PRASS STD PROT HANDLE |
| 00199150023875 - N/A | 2026-02-24 PROBE 8225110 10PK PRASS STD |
| 00199150023882 - N/A | 2026-02-24 PROBE 8225103 5PK PRASS SLIM PROT HANDLE |
| 00763000548797 - Hydrodebrider | 2026-02-23 HYDRODEBRIDER 1914001 STD HANDPIECE ROHS |