LEVEL ONE EXTREMITY

GUDID 00888118133151

BLADE, SCREWDRIVER, IXOS T8, AO

KLS-Martin L.P.

Surgical screwdriver, reusable

• Primary Device ID: 00888118133151
• NIH Device Record Key: 9a66da8f-5594-4f8d-9091-38b4fc10efed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LEVEL ONE EXTREMITY
• Version Model Number: 26-950-16-07
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118133151 [Primary]

FDA Product Code

• HXX: SCREWDRIVER

Sterilization

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

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

[00888118133151]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-04
• Device Publish Date: 2025-02-24

Devices Manufactured by KLS-Martin L.P.

• 00888118145314 - PURE PECTUS: 2026-01-27 INTRODUCER, PEDIATRIC
• 00888118145871 - LEVEL ONE: 2026-01-27 BLADE, SCREWDRIVER, MAXDRIVE, HEX, FOR BOS
• 00888118150271 - IPS: 2025-12-31 IMPLANT, MIDFACE/MANDIBLE, SUPPLEMENTAL, LP, PEEK
• 00888118150608 - RETRACTOR: 2025-12-31 MANDIBULAR, CHANNEL, CHOI
• 00888118140968 - IPS: 2025-12-04 IMPLANT, 1 QUADRANT, PREPROSTHETIC, REMOVABLE MUA, LP, TI-6AL-4V
• 00888118140975 - IPS: 2025-12-04 IMPLANT, 2 QUADRANT, PREPROSTHETIC, REMOVABLE MUA, LP, TI-6AL-4V
• 00888118140982 - IPS: 2025-12-04 IMPLANT, PREPROSTHETIC, SUPPLEMENTAL, REMOVABLE MUA, LP, TI-6AL-4V
• 00888118141804 - IPS: 2025-12-04 IMPLANT, 1 QUADRANT, PREPROSTHETIC, LOCKING, REMOVABLE MUA, LP, TI-6AL-4V