CINELLI OSTEOTOME 475-764

GUDID 00192896042834

CINELLI OSTEOTOME DOUBLE GUARD BLADE

SONTEC INSTRUMENTS, INC.

Plastic surgery osteotome

• Primary Device ID: 00192896042834
• NIH Device Record Key: daedfdef-9a1c-495f-abbf-df87075a0551
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CINELLI OSTEOTOME
• Version Model Number: 475-764
• Catalog Number: 475-764
• 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	00192896042834 [Primary]

FDA Product Code

• HWM: OSTEOTOME

Sterilization

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

[00192896042834]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-07-04
• Device Publish Date: 2018-09-18

On-Brand Devices [CINELLI OSTEOTOME]

• 00192896080249: CINELLI OSTEOTOME WITH FINGER GRIP DOUBLE GUARDED TIPS
• 00192896080232: CINELLI OSTEOTOME WITH FINGER GRIP DOUBLE GUARDED TIPS
• 00192896042841: CINELLI OSTEOTOME DOUBLE GUARD BLADE
• 00192896042834: CINELLI OSTEOTOME DOUBLE GUARD BLADE
• 00192896042827: CINELLI OSTEOTOME DOUBLE GUARD BLADE
• 00192896042810: CINELLI OSTEOTOME DOUBLE GUARD BLADE