Palpation Nerve Hook TNH152548

GUDID 04250337120506

NiTi Palpation Nerve Hook, superelastic

Joimax GmbH

Nerve/vessel retractor
Primary Device ID04250337120506
NIH Device Record Key7506dc11-ab92-4ad1-b163-9a66dede0c15
Commercial Distribution StatusIn Commercial Distribution
Brand NamePalpation Nerve Hook
Version Model NumberTNH152548
Catalog NumberTNH152548
Company DUNS344267187
Company NameJoimax GmbH
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com
Phone+497212551407010
Emailinfo@joimax.com

Device Dimensions

Device Size Text, specify0
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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104250337120506 [Primary]

FDA Product Code

GFIOsteotome, Manual

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


[04250337120506]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-09
Device Publish Date2023-09-29

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