BLOCK, STERILE

GUDID 00888118089120

KLS-Martin L.P.

Surgical instrument/implant rack

• Primary Device ID: 00888118089120
• NIH Device Record Key: 158c6bfe-402d-4ebe-ba55-929680497334
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BLOCK, STERILE
• Version Model Number: 55-969-91-71
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118089120 [Primary]

FDA Product Code

• JXS: BLOCK, CUTTING, ENT, STERILE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-08-23
• Device Publish Date: 2018-09-26

Devices Manufactured by KLS-Martin L.P.

• 00888118141996 - L1: 2024-02-29
• 00888118142092 - L1 STERNAL: 2024-02-29
• 00888118142108 - L1 LINOS: 2024-02-29
• 00888118142115 - L1 LINOS: 2024-02-29
• 00888118142122 - L1 LINOS: 2024-02-29
• 00888118142993 - IPS: 2024-02-29
• 00888118143006 - IPS: 2024-02-29
• 00888118143013 - IPS: 2024-02-29