10732 Dual Tip Skin Marker; Regular/Fine Tip Gentian Violet; w/Ruler and Labels 10732

GUDID 20787551008528

10732 Dual Tip Skin Marker; Regular and Fine Tip Gentian Violet; w/ Ruler and Labels

XODUS MEDICAL, INC.

Skin marking pen, single-use

• Primary Device ID: 20787551008528
• NIH Device Record Key: c2f9bb74-d517-4306-81c0-21e3c81a5cf6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 10732 Dual Tip Skin Marker; Regular/Fine Tip Gentian Violet; w/Ruler and Labels
• Version Model Number: 10732
• Catalog Number: 10732
• Company DUNS: 868042664
• Company Name: XODUS MEDICAL, INC.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00787551008524 [Primary]
GS1	20787551008528 [Package]; Contains: 00787551008524; Package: CASE [100 Units]; In Commercial Distribution

FDA Product Code

• FZZ: MARKER, SKIN

Sterilization

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

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

[20787551008528]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-10-17
• Device Publish Date: 2022-12-13

Devices Manufactured by XODUS MEDICAL, INC.

• 20787551011917 - 10203 Coated Ruler Printed: 2024-09-11 10203 Coated Ruler Printed
• 20787551011931 - NS10203 Coated Ruler Printed #4000 8PT C1S: 2024-09-11 NS10203 Coated Ruler Printed #4000 8PT C1S
• 20787551006104 - 50300 EZ Cover Foot Pedal Bag w/ Large Button: 2024-07-25 50300 EZ Cover Foot Pedal Bag w/ Large Button
• 20787551039744 - 40680 The Pink Pad - Advanced Trendelenburg Positioning Kit - Biodegradable: 2024-07-25 40680 The Pink Pad - Advanced Trendelenburg Positioning Kit - Biodegradable
• 20787551040696 - SPK10251 Specialty Positioning Kit: 2024-07-25 SPK10251 Specialty Positioning Kit
• 20787551040702 - NSCL25278 Custom Med Label Pack: 2024-07-25 NSCL25278 Custom Med Label Pack
• 20787551040719 - SPK11538 Surgical BackPack Kit: 2024-07-25 SPK11538 Surgical BackPack Kit
• 20787551040726 - RTK10562 Room Turn-Over Kit: 2024-07-25 RTK10562 Room Turn-Over Kit