GILLS-WELSH ASPRIRATING CANNULA 16-5670

GUDID 00192896075030

GILLS-WELSH ASPRIRATING CANNULA BLUNT ANGLED SMOOTH TIP

SONTEC INSTRUMENTS, INC.

Ophthalmic working-channel cannula, reusable

• Primary Device ID: 00192896075030
• NIH Device Record Key: 8b1f86d8-2065-415c-a62e-a7080764aa2b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GILLS-WELSH ASPRIRATING CANNULA
• Version Model Number: 16-5670
• Catalog Number: 16-5670
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• 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(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Needle Gauge: 25 Gauge
• Needle Gauge: 25 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896075030 [Primary]

FDA Product Code

• HMX: Cannula, ophthalmic

Sterilization

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

[00192896075030]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-22
• Device Publish Date: 2018-09-20

On-Brand Devices [GILLS-WELSH ASPRIRATING CANNULA]

• 00192896075047: GILLS-WELSH ASPRIRATING CANNULA BLUNT ANGLED SMOOTH TIP
• 00192896075030: GILLS-WELSH ASPRIRATING CANNULA BLUNT ANGLED SMOOTH TIP
• 00192896075023: GILLS-WELSH ASPRIRATING CANNULA BLUNT ANGLED SMOOTH TIP