| Primary Device ID | 00643169101982 |
| NIH Device Record Key | a29fb117-b44e-4aa4-8981-6c82c6a16b1a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Quadcut® |
| Version Model Number | 1883080HRE |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | 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 | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Outer Diameter | 3 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169101982 [Primary] |
| EQJ | BUR, EAR, NOSE AND THROAT |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-09-10 |
| 00613994779199 | BLADE 1884380HRE QUADCUT 4.3MM X 13CM |
| 20613994779186 | BLADE 1884380HR QUADCUT 5PK 4.3MM X 13CM |
| 00643169101999 | BLADE 1883480HRE QUADCUT 3.4MM X 13CM |
| 00643169101982 | BLADE 1883080HRE QUADCUT 3.0MM X 13CM |
| 20763000038162 | BLADE 1884380HR QUADCUT 5PK 4.3MM X 13CM |
| 00763000033989 | BLADE 1883080HRE QUADCUT 3.0MM X 13CM |
| 00763000033910 | BLADE 1884380HRE QUADCUT 4.3MM X 13CM |
| 00763000033996 | BLADE 1883480HRE QUADCUT 3.4MM X 13CM |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() QUADCUT 85067363 3942261 Live/Registered |
Medtronic Xomed, Inc. 2010-06-21 |