Quadcut®

GUDID 00643169101982

BLADE 1883080HRE QUADCUT 3.0MM X 13CM

MEDTRONIC XOMED, INC.

Oscillating surgical saw blade, single-use Oscillating surgical saw blade, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use Surgical saw blade, oscillating, single-use
Primary Device ID00643169101982
NIH Device Record Keya29fb117-b44e-4aa4-8981-6c82c6a16b1a
Commercial Distribution StatusIn Commercial Distribution
Brand NameQuadcut®
Version Model Number1883080HRE
Company DUNS835465063
Company NameMEDTRONIC XOMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter
Outer Diameter3 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169101982 [Primary]

FDA Product Code

EQJBUR, EAR, NOSE AND THROAT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-09-10

On-Brand Devices [Quadcut®]

00613994779199BLADE 1884380HRE QUADCUT 4.3MM X 13CM
20613994779186BLADE 1884380HR QUADCUT 5PK 4.3MM X 13CM
00643169101999BLADE 1883480HRE QUADCUT 3.4MM X 13CM
00643169101982BLADE 1883080HRE QUADCUT 3.0MM X 13CM
20763000038162BLADE 1884380HR QUADCUT 5PK 4.3MM X 13CM
00763000033989BLADE 1883080HRE QUADCUT 3.0MM X 13CM
00763000033910BLADE 1884380HRE QUADCUT 4.3MM X 13CM
00763000033996BLADE 1883480HRE QUADCUT 3.4MM X 13CM

Trademark Results [Quadcut]

Mark Image

Registration | Serial
Company
Trademark
Application Date
QUADCUT
QUADCUT
85067363 3942261 Live/Registered
Medtronic Xomed, Inc.
2010-06-21

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.