BECHERT LENS ROTATOR 12-2700

GUDID 00192896072695

BECHERT LENS ROTATOR BLUNT FORKED ANGLED TIP

SONTEC INSTRUMENTS, INC.

Lens loop, reusable

• Primary Device ID: 00192896072695
• NIH Device Record Key: 4df21062-53ac-45a1-b712-0a9e4b1c6935
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BECHERT LENS ROTATOR
• Version Model Number: 12-2700
• Catalog Number: 12-2700
• 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: 11 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896072695 [Primary]

FDA Product Code

• HND: Spatula, ophthalmic

Sterilization

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

[00192896072695]

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: 2018-09-19

On-Brand Devices [BECHERT LENS ROTATOR]

• 00192896072725: BECHERT LENS ROTATOR BLUNT ANGLED FORKED TIP TITANIUM
• 00192896072695: BECHERT LENS ROTATOR BLUNT FORKED ANGLED TIP