Palpation Nerve Hook TNH152548

GUDID 04250337120506

NiTi Palpation Nerve Hook, superelastic

Joimax GmbH

Nerve/vessel retractor

• Primary Device ID: 04250337120506
• NIH Device Record Key: 7506dc11-ab92-4ad1-b163-9a66dede0c15
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Palpation Nerve Hook
• Version Model Number: TNH152548
• Catalog Number: TNH152548
• 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: false
• 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	04250337120506 [Primary]

FDA Product Code

• GFI: Osteotome, Manual

Sterilization

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

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

Moist Heat or Steam Sterilization

[04250337120506]

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

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