CATHETER

GUDID 00888118057709

KLS-Martin L.P.

Eustachian catheter, reusable

• Primary Device ID: 00888118057709
• NIH Device Record Key: 5dd095c1-1c55-4428-85a2-663994c3712b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CATHETER
• Version Model Number: 36-321-03-01
• 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	00888118057709 [Primary]

FDA Product Code

• GBY: CATHETER, EUSTACHIAN, GENERAL & PLASTIC SURGERY

Sterilization

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

[00888118057709]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-20
• Device Publish Date: 2018-09-26

On-Brand Devices [CATHETER]

• 00888118057709: 36-321-03-01
• 00888118057693: 36-321-02-01
• 00888118057686: 36-321-01-01