CANNULA

GUDID 00888118055828

KLS-Martin L.P.

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

• Primary Device ID: 00888118055828
• NIH Device Record Key: 8fe7781d-d715-4d06-b00e-ce9135275d1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CANNULA
• Version Model Number: 34-975-30-01
• 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	00888118055828 [Primary]

FDA Product Code

• HMX: Cannula, ophthalmic

Sterilization

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

[00888118055828]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-10-07
• Device Publish Date: 2018-09-26

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