Typhoon™ Infinite Flex NiTi Files 20/.04 (31mm) 312341

GUDID 07540172014304

Endodontic surgical files

CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.

Rotary/reciprocating endodontic file/rasp, reusable

• Primary Device ID: 07540172014304
• NIH Device Record Key: bc7718b2-1814-4057-9627-46ba3da751f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Typhoon™ Infinite Flex NiTi Files 20/.04 (31mm)
• Version Model Number: 312341
• Catalog Number: 312341
• Company DUNS: 626406016
• Company Name: CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com
• Phone: +1(800)265-3444
• Email: info@clinicianschoice.com

Device Dimensions

• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter
• Device Size Text, specify: 0
• Length: 31 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07540172014304 [Primary]

FDA Product Code

• EKS: FILE, PULP CANAL, ENDODONTIC

Sterilization

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

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

[07540172014304]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-25
• Device Publish Date: 2020-03-17