L1 RECONGUIDE

GUDID 00888118123855

KLS-Martin L.P.

Surgical implant template, reusable

• Primary Device ID: 00888118123855
• NIH Device Record Key: de096f4c-2a45-4839-84d6-5e5b0d039bbe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: L1 RECONGUIDE
• Version Model Number: 25-500-26-07
• Company DUNS: 826499238
• Company Name: KLS-Martin L.P.
• 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: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118123855 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

[00888118123855]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-12-30
• Device Publish Date: 2019-12-20

On-Brand Devices [L1 RECONGUIDE]

• 00888118123947: 25-500-35-07
• 00888118123930: 25-407-10-04
• 00888118123923: 25-500-33-07
• 00888118123916: 25-500-32-07
• 00888118123909: 25-500-31-07
• 00888118123893: 25-500-30-07
• 00888118123886: 25-500-29-07
• 00888118123879: 25-500-28-07
• 00888118123862: 25-500-27-07
• 00888118123855: 25-500-26-07
• 00888118123848: 25-500-25-07
• 00888118123831: 25-500-24-07
• 00888118123824: 25-500-23-07
• 00888118123817: 25-500-22-07
• 00888118123800: 25-500-21-07
• 00888118123794: 25-500-07-07
• 00888118123787: 25-500-06-07
• 00888118123770: 25-500-05-07
• 00888118123763: 25-500-04-07
• 00888118123756: 25-500-03-07
• 00888118123749: 25-500-02-07
• 00888118123732: 25-500-01-07
• 00888118122094: 25-500-20-07
• 00888118122087: 25-500-00-07
• 00888118123978: 55-990-53-04
• 00888118123961: 55-990-52-04
• 00888118123954: 55-990-51-04
• 00888118128119: DRILL GUIDE, 2.0 MM, W/HANDLE
• 00888118128102: HANDLE, SCREWDRIVER, FLAT, BLACK, 2.0/2.3 MM SCREW