Splinter Forceps

GUDID 00192896102576

Feilchenfeld Splinter Forceps

SONTEC INSTRUMENTS, INC.

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

• Primary Device ID: 00192896102576
• NIH Device Record Key: cf88e513-647e-43af-a65c-d486de8796e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Splinter Forceps
• Version Model Number: 138-020
• 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
• 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 Dimensions

• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch
• Length: 3 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]
GS1	00192896102576 [Primary]

FDA Product Code

• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS
• HTD: FORCEPS

Sterilization

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

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896102576]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-06-23
• Device Publish Date: 2020-06-15

On-Brand Devices [Splinter Forceps]

• 00192896023338: SPLINTER FORCEPS ANGLED TIP
• 00192896102583: Carmalt Splinter Forceps Curved Tip
• 00192896102576: Feilchenfeld Splinter Forceps