Primary Device ID | 00763000579241 |
NIH Device Record Key | c6f0f79f-5ebe-4d87-9501-8f05e91891b2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Quadcut |
Version Model Number | 1884080EM |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
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 | 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 |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Outer Diameter | 4 Millimeter |
Length | 13 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000579241 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-01-28 |
Device Publish Date | 2022-01-20 |
00763000579272 | BLADE 1884380EM QUADCUT 4.3MMX13CM ROHS |
00763000579265 | BLADE 1883480EM QUADCUT 3.4MMX13CM ROHS |
00763000579241 | BLADE 1884080EM TRICUT 4MMX13CM M4 ROHS |
00763000579234 | BLADE 1884012EM RAD12 4MM M4 ROTATE ROHS |
00763000579227 | BLADE 1884006EM RAD40 4MM M4 ROTATE ROHS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
QUADCUT 85067363 3942261 Live/Registered |
Medtronic Xomed, Inc. 2010-06-21 |