Guiding Tube GTC212564

GUDID 04250337120391

Guiding Tube, conical, yellow

Joimax GmbH

Endoscope sheath, reusable
Primary Device ID04250337120391
NIH Device Record Keya2cc9dd6-ea1a-436c-83e0-36de46c97ed9
Commercial Distribution StatusIn Commercial Distribution
Brand NameGuiding Tube
Version Model NumberGTC212564
Catalog NumberGTC212564
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 Numbertrue
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
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 Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104250337120391 [Primary]

FDA Product Code

FZXGuide, Surgical, Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

Moist Heat or Steam Sterilization


[04250337120391]

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

On-Brand Devices [Guiding Tube]

04250337120407Guiding Tube, conical, red
04250337120391Guiding Tube, conical, yellow

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