Guiding Tube GTC212564

GUDID 04250337120391

Guiding Tube, conical, yellow

Joimax GmbH

Endoscope sheath, reusable

• Primary Device ID: 04250337120391
• NIH Device Record Key: a2cc9dd6-ea1a-436c-83e0-36de46c97ed9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guiding Tube
• Version Model Number: GTC212564
• Catalog Number: GTC212564
• Company DUNS: 344267187
• Company Name: Joimax GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250337120391 [Primary]

FDA Product Code

• FZX: Guide, Surgical, Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[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 Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-09
• Device Publish Date: 2023-09-29

On-Brand Devices [Guiding Tube]

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