Working Tube WTS709304

GUDID 04250337120384

Working Tube with sealing, straight 90°

Joimax GmbH

Endoscope sheath, reusable
Primary Device ID04250337120384
NIH Device Record Key9dcfa8d9-c776-4497-8fb4-1173513bf520
Commercial Distribution StatusIn Commercial Distribution
Brand NameWorking Tube
Version Model NumberWTS709304
Catalog NumberWTS709304
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
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
GS104250337120384 [Primary]

FDA Product Code

GDFGuide, Needle, Surgical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

Moist Heat or Steam Sterilization


[04250337120384]

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 [Working Tube]

04250337120384Working Tube with sealing, straight 90°
04250337120377Working Tube with sealing, Standard Lip
04250337120360Working Tube with sealing, straight 90°
04250337120353Working Tube with sealing, Standard Lip

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.