guide wire JPGW38015

GUDID 04250337114239

Guide Wire with markers, straight, non-sterile

Joimax GmbH

Orthopaedic bone wire

• Primary Device ID: 04250337114239
• NIH Device Record Key: fda419ec-d6c0-4526-9a72-211819b926e8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: guide wire
• Version Model Number: JPGW38015
• Catalog Number: JPGW38015
• Company DUNS: 344267187
• Company Name: Joimax GmbH
• Device Count: 1
• DM Exempt: true
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250337114239 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[04250337114239]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-19
• Device Publish Date: 2022-12-30

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