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 |