Indian Knife IK150610

GUDID 04250337120476

Indian Knife with handle

Joimax GmbH

Bone lever/elevator, reusable

• Primary Device ID: 04250337120476
• NIH Device Record Key: 39fb0862-39c1-48a6-aad6-4f5e5679e6d9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Indian Knife
• Version Model Number: IK150610
• Catalog Number: IK150610
• 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	04250337120476 [Primary]

FDA Product Code

• FZS: Curette, Surgical, General Use

Sterilization

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

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

Moist Heat or Steam Sterilization

[04250337120476]

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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• 04250337118640 - Vaporace® Probe bipolar, Area 320 mm – 3.5 mm: 2025-02-24
• 04250337118978 - Vaporace® Hand Piece, bipolar: 2025-02-24
• 04250337120230 - Vaporace® Probe bipolar, Area 150 mm – 3.5 mm: 2025-02-24
• 04250337101741 - iLESSYS®: 2024-09-11 TESSYS® Steel Ruler
• 04250337102854 - Adapter: 2024-07-15 Lightsource Adaptor for Foraminoscope (Wolf)
• 04250337102861 - Adapter: 2024-07-15 Lightsource Adaptor for Foraminoscope (Storz)