guide wire JPGW38015

GUDID 04250337114239

Guide Wire with markers, straight, non-sterile

Joimax GmbH

Orthopaedic bone wire
Primary Device ID04250337114239
NIH Device Record Keyfda419ec-d6c0-4526-9a72-211819b926e8
Commercial Distribution StatusIn Commercial Distribution
Brand Nameguide wire
Version Model NumberJPGW38015
Catalog NumberJPGW38015
Company DUNS344267187
Company NameJoimax GmbH
Device Count1
DM Exempttrue
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104250337114239 [Primary]

FDA Product Code

FZXGuide, surgical, instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337114239]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-02-19
Device Publish Date2022-12-30

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04250337101338joimax® Guide Wires

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