Octopus™

GUDID 00763000284800

RETRACTOR ADPTR 28045 OCTOPUS

MEDTRONIC, INC.

Rib spreader, reusable Rib spreader, reusable Rib spreader, reusable Rib spreader, reusable Rib spreader, reusable Rib spreader, reusable Rib spreader, reusable Rib spreader, reusable
Primary Device ID00763000284800
NIH Device Record Keyad29c44a-6ccf-4861-a43b-b79aede905ac
Commercial Distribution StatusIn Commercial Distribution
Brand NameOctopus™
Version Model Number28045
Company DUNS006261481
Company NameMEDTRONIC, 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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000284800 [Primary]
GS100763000284800 [Primary]
GS100763000284800 [Primary]
GS100763000284800 [Primary]
GS100763000284800 [Primary]
GS100763000284800 [Primary]
GS100763000284800 [Primary]
GS100763000284800 [Primary]

FDA Product Code

MWSStabilizer, heart
MWSStabilizer, heart
MWSStabilizer, heart
MWSStabilizer, heart
MWSStabilizer, heart
MWSStabilizer, heart
MWSStabilizer, heart
MWSStabilizer, heart

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00763000284800]

Moist Heat or Steam Sterilization


[00763000284800]

Moist Heat or Steam Sterilization


[00763000284800]

Moist Heat or Steam Sterilization


[00763000284800]

Moist Heat or Steam Sterilization


[00763000284800]

Moist Heat or Steam Sterilization


[00763000284800]

Moist Heat or Steam Sterilization


[00763000284800]

Moist Heat or Steam Sterilization


[00763000284800]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-09
Device Publish Date2020-10-30

Devices Manufactured by MEDTRONIC, INC.

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00763000178130 - Cobalt™ XT HF CRT-D MRI SureScan™2020-11-30 CRTD DTPA2D4 COBALT XT HF MRI DF4
00763000178147 - Cobalt™ XT HF CRT-D MRI SureScan™2020-11-30 CRTD DTPA2D1 COBALT XT HF MRI DF1
00763000178338 - Cobalt™ XT DR MRI SureScan™2020-11-30 ICD DDPA2D1 COBALT XT DR MRI DF1
00763000178345 - Cobalt™ XT DR MRI SureScan™2020-11-30 ICD DDPA2D4 COBALT XT DR MRI DF4
00763000178451 - Cobalt™ XT VR MRI SureScan™2020-11-30 ICD DVPA2D1 COBALT XT VR MRI DF1
00763000178468 - Cobalt™ XT VR MRI SureScan™2020-11-30 ICD DVPA2D4 COBALT XT VR MRI DF4

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