WILDER LACRIMAL DILATOR 16-2470

GUDID 00192896018495

WILDER LACRIMAL DILATOR SINGLE ENDED MEDIUM TIP #2

SONTEC INSTRUMENTS, INC.

Lacrimal dilator, reusable

• Primary Device ID: 00192896018495
• NIH Device Record Key: b79b7f39-7854-450f-8e7b-36d165cf2ece
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WILDER LACRIMAL DILATOR
• Version Model Number: 16-2470
• Catalog Number: 16-2470
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00192896018495 [Primary]

FDA Product Code

• HNW: Dilator, lachrymal

Sterilization

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

[00192896018495]

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: 2018-10-18
• Device Publish Date: 2018-09-17

On-Brand Devices [WILDER LACRIMAL DILATOR]

• 00192896018501: WILDER LACRIMAL DILATOR SINGLE ENDED HEAVY TIP #3
• 00192896018495: WILDER LACRIMAL DILATOR SINGLE ENDED MEDIUM TIP #2
• 00192896018488: WILDER LACRIMAL DILATOR SINGLE ENDEDFINE TIP #1