WILDER LENS LOOP 12-4402

GUDID 00192896013506

WILDER LENS LOOP CURVED SERRATED LOOP STAINLESS STEEL

SONTEC INSTRUMENTS, INC.

Lens loop, reusable

• Primary Device ID: 00192896013506
• NIH Device Record Key: de54a004-75ea-4211-9703-21b41d77470e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WILDER LENS LOOP
• Version Model Number: 12-4402
• Catalog Number: 12-4402
• 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

• Length: 5.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896013506 [Primary]

FDA Product Code

• HND: Spatula, ophthalmic

Sterilization

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

[00192896013506]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-10-07
• Device Publish Date: 2018-09-18

On-Brand Devices [WILDER LENS LOOP]

• 00192896072787: WILDER LENS LOOP STRAIGHT SERRATED LOOP STAINLESS STEEL
• 00192896013506: WILDER LENS LOOP CURVED SERRATED LOOP STAINLESS STEEL