UBE Triangulation Tool UTA4015

GUDID 04250337120582

UBE Triangulation Tool

Joimax GmbH

Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable Needle guide, reusable
Primary Device ID04250337120582
NIH Device Record Key5b71b0fa-6c87-47e5-8c39-330669005717
Commercial Distribution StatusIn Commercial Distribution
Brand NameUBE Triangulation Tool
Version Model NumberUTA4015
Catalog NumberUTA4015
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

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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 Identifiers

Device Issuing AgencyDevice ID
GS104250337120582 [Primary]

FDA Product Code

HRRScissors, Orthopedic, Surgical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

Moist Heat or Steam Sterilization


[04250337120582]

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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04250337101376 - guide wire2024-02-19 joimax® Guide Wire, super elastic, unsterile
04250337112440 - guide wire2024-02-19 Guide Wire with marker, straight, non-sterile
04250337112945 - guide wire2024-02-19 joimax® Guide Wire, super elastic, unsterile
04250337114154 - guide wire2024-02-19 joimax® Guide Wire super elastic, nonsterile
04250337114239 - guide wire2024-02-19 Guide Wire with markers, straight, non-sterile
04250337120124 - Bone Resector2023-10-09 Bone Resector, Ball Tip

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