BAYONET CURETTE 413-040

GUDID 00192896036758

BAYONET CURETTE BENDING HYPOPHYSIS ENUCLEATOR TITANIUM

SONTEC INSTRUMENTS, INC.

General-purpose curette

• Primary Device ID: 00192896036758
• NIH Device Record Key: fae9c6f9-3c31-4389-aa9b-8c7c66a9388d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BAYONET CURETTE
• Version Model Number: 413-040
• Catalog Number: 413-040
• 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: 8.75 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896036758 [Primary]

FDA Product Code

• HTF: CURETTE

Sterilization

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

[00192896036758]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-09-10
• Device Publish Date: 2018-09-13

On-Brand Devices [BAYONET CURETTE]

• 00192896079199: BAYONET CURETTE DOWN ANGLE RING TIP TITANIUM
• 00192896079182: BAYONET CURETTE UP-ANGLE RING TIP TITANIUM
• 00192896036758: BAYONET CURETTE BENDING HYPOPHYSIS ENUCLEATOR TITANIUM
• 00192896104136: Bayonet Curette Knurled Handle 45 Degree Up Angle Titanium
• 00192896104853: Bayonet Curette Knurl Handle 45 Degrees Up Angle Titanium
• 00192896104846: Bayonet Curette Knurl Handle 90 Degree Up AngleTitanium