KIRLAND PERIODONTAL CURETTE 1102-CPK13-13L

GUDID 00192896050082

KIRLAND PERIODONTAL CURETTE #13-13L DOUBLE ENDED BLADES STANDARD HANDLE

SONTEC INSTRUMENTS, INC.

Periodontal curette

• Primary Device ID: 00192896050082
• NIH Device Record Key: d5524f51-fdc1-4748-97eb-cad406284ca6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KIRLAND PERIODONTAL CURETTE
• Version Model Number: 1102-CPK13-13L
• Catalog Number: 1102-CPK13-13L
• 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

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896050082 [Primary]

FDA Product Code

• EMH: FORCEPS, RONGEUR, SURGICAL
• EMK: Curette, Surgical, Dental

Sterilization

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

[00192896050082]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2019-09-06
• Device Publish Date: 2018-09-17

On-Brand Devices [KIRLAND PERIODONTAL CURETTE]

• 00192896082304: KIRLAND PERIODONTAL CURETTE #13-13L DOUBLE ENDED BLADES LIGHT HANDLE
• 00192896050082: KIRLAND PERIODONTAL CURETTE #13-13L DOUBLE ENDED BLADES STANDARD HANDLE