Awl Set

GUDID 04057217006703

Z-Medical GmbH + Co. KG

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• Primary Device ID: 04057217006703
• NIH Device Record Key: d2feb757-e2b4-4a06-885a-0d181d81d4de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Awl Set
• Version Model Number: A06 530
• Company DUNS: 332068761
• Company Name: Z-Medical GmbH + Co. KG
• 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: false
• 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: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de
• Phone: +497462945540
• Email: info@z-medical.de

Device Identifiers

Device Issuing Agency	Device ID
GS1	04057217006703 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

[04057217006703]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-09
• Device Publish Date: 2024-04-01

Devices Manufactured by Z-Medical GmbH + Co. KG

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• 04057217000022 - Z-Pedicle Screw: 2024-04-09
• 04057217000039 - Z-Pedicle Screw: 2024-04-09
• 04057217000046 - Z-Pedicle Screw: 2024-04-09
• 04057217000053 - Z-Pedicle Screw: 2024-04-09
• 04057217000060 - Z-Pedicle Screw: 2024-04-09
• 04057217000077 - Z-Pedicle Screw: 2024-04-09
• 04057217000084 - Z-Pedicle Screw: 2024-04-09