One-way valve for working tube CVALVE2020

GUDID 04250337120742

Joimax GmbH

Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable Endoscope sheath, reusable
Primary Device ID04250337120742
NIH Device Record Keyfd2386b2-b716-475f-bd04-92b28cdedf9f
Commercial Distribution StatusIn Commercial Distribution
Brand NameOne-way valve for working tube
Version Model NumberCVALVE2020
Catalog NumberCVALVE2020
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 Identifiers

Device Issuing AgencyDevice ID
GS104250337120742 [Primary]

FDA Product Code

GDFGuide, Needle, Surgical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

Moist Heat or Steam Sterilization

[04250337120742]

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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04250337120124 - Bone Resector2023-10-09 Bone Resector, Ball Tip
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