REPLACEMENT BLADE 1100-500

GUDID 00192896081512

REPLACEMENT BLADE

SONTEC INSTRUMENTS, INC.

Manual surgical saw blade, rigid

• Primary Device ID: 00192896081512
• NIH Device Record Key: 9089f4aa-e61f-4cc4-92b9-b66aaa013314
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REPLACEMENT BLADE
• Version Model Number: 1100-500
• Catalog Number: 1100-500
• 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 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896081512 [Primary]

FDA Product Code

• GDR: SAW, MANUAL AND ACCESSORIES

Sterilization

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

[00192896081512]

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: 2018-10-22
• Device Publish Date: 2018-09-20

On-Brand Devices [REPLACEMENT BLADE]

• 00192896081512: REPLACEMENT BLADE
• 00192896024618: REPLACEMENT BLADE FOR FINGER RING CUTTER SAW