Arruga Capsule Forceps T14-7300

GUDID 00192896117457

Arruga Capsule Forceps New Curve Tip Titanium

SONTEC INSTRUMENTS, INC.

Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

• Primary Device ID: 00192896117457
• NIH Device Record Key: f0e45eee-a4d9-47a1-8d2a-9a5c90a5630e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arruga Capsule Forceps
• Version Model Number: T14-7300
• Catalog Number: T14-7300
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896117457 [Primary]

FDA Product Code

• HNR: Forceps, ophthalmic

Sterilization

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

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

[00192896117457]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-07
• Device Publish Date: 2024-04-29

On-Brand Devices [Arruga Capsule Forceps]

• 00192896016996: ARRUGA CAPSULE FORCEPS STANDARD CURVE TIP
• 00192896016989: ARRUGA CAPSULE FORCEPS NEW CURVED TIP
• 00192896117457: Arruga Capsule Forceps New Curve Tip Titanium