CANNULA

GUDID 00888118121981

KLS-Martin L.P.

ENT suction dissector

• Primary Device ID: 00888118121981
• NIH Device Record Key: fb0a28cd-2d23-47b9-b92a-8b1139335b86
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CANNULA
• Version Model Number: 18-640-20-01
• 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: webcontact@klsmartin.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118121981 [Primary]

FDA Product Code

• GEA: CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

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

[00888118121981]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-07-03
• Device Publish Date: 2019-06-25

On-Brand Devices [CANNULA]

• 00888118055828: 34-975-30-01
• 00888118055811: 34-975-20-01
• 00888118055804: 34-975-10-01
• 00888118055798: 34-975-00-01
• 00888118121981: 18-640-20-01
• 00888118122018: 18-640-20-07
• 00888118116826: 37-816-30-07
• 00888118116819: 37-814-30-07
• 00888118097248: 99-563-40-02
• 00888118096371: 50-501-24-07
• 00888118062666: 38-550-31-07
• 00888118061065: 37-815-30-02