DIRECTOR

GUDID 00888118022882

KLS-Martin L.P.

Fistula probe

• Primary Device ID: 00888118022882
• NIH Device Record Key: 081d8c8f-f5ce-4917-a68d-cf72c962e90a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIRECTOR
• Version Model Number: 16-160-13-01
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118022882 [Primary]

FDA Product Code

• FGM: PROBE AND DIRECTOR, GASTRO-UROLOGY

Sterilization

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

[00888118022882]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-21
• Device Publish Date: 2018-09-26

On-Brand Devices [DIRECTOR]

• 00888118122445: 38-684-39-07
• 00888118122346: 38-684-29-07
• 00888118122315: 38-684-25-07
• 00888118118912: 99-559-65-01
• 00888118064677: 39-311-20-07
• 00888118064660: 39-311-19-07
• 00888118064653: 39-309-18-07
• 00888118022936: 16-170-16-01
• 00888118022929: 16-170-14-01
• 00888118022912: 16-170-13-01
• 00888118022905: 16-160-16-01
• 00888118022899: 16-160-14-01
• 00888118022882: 16-160-13-01
• 00888118022875: 16-160-11-01
• 00888118011046: 09-453-18-07