FOREMANN K-WIRE DISTRACTOR 417-062A

GUDID 00192896037922

FOREMANN K-WIRE DISTRACTOR SMALL OUTSPREAD ARMS

SONTEC INSTRUMENTS, INC.

Orthopaedic surgical distractor, internal

• Primary Device ID: 00192896037922
• NIH Device Record Key: 4c615c61-43da-44e3-8a74-9fa572279b47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FOREMANN K-WIRE DISTRACTOR
• Version Model Number: 417-062A
• Catalog Number: 417-062A
• 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: 6 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896037922 [Primary]

FDA Product Code

• HWN: INSTRUMENT, COMPRESSION

Sterilization

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

[00192896037922]

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: 2018-10-15
• Device Publish Date: 2018-09-13

On-Brand Devices [FOREMANN K-WIRE DISTRACTOR]

• 00192896037953: FOREMANN K-WIRE DISTRACTOR TAPERED ARMS
• 00192896037946: FOREMANN K-WIRE DISTRACTOR LARGE OUTSPREAD ARMS
• 00192896037939: FOREMANN K-WIRE DISTRACTOR LARGE CLOSED ARMS
• 00192896037922: FOREMANN K-WIRE DISTRACTOR SMALL OUTSPREAD ARMS
• 00192896037915: FOREMANN K-WIRE DISTRACTOR SMALL CLOSED ARMS