FILTER

GUDID 00888118061355

KLS-Martin L.P.

Bone graft harvesting filter

• Primary Device ID: 00888118061355
• NIH Device Record Key: 40fbe171-1152-4a50-a268-38fb6c1aae1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FILTER
• Version Model Number: 38-025-01-07
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118061355 [Primary]

FDA Product Code

• MXP: BONE PARTICLE COLLECTOR

Sterilization

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

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

[00888118061355]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-22
• Device Publish Date: 2018-09-26

Devices Manufactured by KLS-Martin L.P.

• 00888118143105 - MIRROR: 2024-12-03 LARYNGEAL, NO. 3, 16.5 MM DIAMETER, RHODIUM PLATED
• 00888118143112 - MIRROR: 2024-12-03 LARYNGEAL, NO. 4, 18.5 MM DIAMETER, RHODIUM PLATED
• 00888118143129 - MIRROR: 2024-12-03 LARYNGEAL, NO. 6, 22.5 MM DIAMETER, RHODIUM PLATED
• 00888118143136 - MIRROR: 2024-12-03 LARYNGEAL, NO. 7, 24.5 MM DIAMETER, RHODIUM PLATED
• 00888118143143 - MIRROR: 2024-12-03 LARYNGEAL, NO. 8, 26.5 MM DIAMETER, RHODIUM PLATED
• 00888118143150 - MIRROR: 2024-12-03 LARYNGEAL, NO. 10, 30.5 MM DIAMETER, RHODIUM PLATED
• 00888118145024 - IPS: 2024-12-03 IMPLANT, 1 QUADRANT, PREPROSTHETIC, MUA, LP, CAN, TI-6AL-4V
• 00888118145031 - IPS: 2024-12-03 IMPLANT, 2 QUADRANT, PREPROSTHETIC, MUA, LP, CAN, TI-6AL-4V