GUDID 20613994802501

PROBE PSP1001 10PK 175MM PEDI SCREW ROHS

MEDTRONIC XOMED, INC.

Nerve-locating system, line-powered Nerve-locating system, line-powered
Primary Device ID20613994802501
NIH Device Record Key827f13b1-5c7e-4d2e-bfda-510e28ef1fc0
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberPSP1001
Company DUNS835465063
Company NameMEDTRONIC XOMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

Device Dimensions

Length175 Millimeter
Length175 Millimeter
Length175 Millimeter
Length175 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100613994802507 [Primary]
GS120613994802501 [Package]
Contains: 00613994802507
Package: PK [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GXZELECTRODE, NEEDLE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-04-30

Devices Manufactured by MEDTRONIC XOMED, INC.

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00763000036621 - Big Easy® Piston2024-05-20 PROSTHESIS 1156621 PLAT/TI .5X4.5MM RT
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