SNARE

GUDID 00888118057723

KLS-Martin L.P.

Nasal snare, reusable

• Primary Device ID: 00888118057723
• NIH Device Record Key: 73bfc658-7a0a-4d1e-b9ec-a877cafb8693
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SNARE
• Version Model Number: 36-353-16-07
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118057723 [Primary]

FDA Product Code

• JZD: SNARE, EAR

Sterilization

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

[00888118057723]

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

On-Brand Devices [SNARE]

• 10888118064780: 39-513-01-07
• 10888118064773: 39-511-50-07
• 00888118064790: 39-525-01-07
• 00888118064769: 39-506-28-07
• 00888118064752: 39-502-28-07
• 00888118064745: 39-500-28-07
• 00888118058744: 36-899-12-01
• 00888118058737: 36-885-26-07
• 00888118057723: 36-353-16-07
• 00888118057716: 36-351-16-07