HOUSE GELFOAM PRESS 468-531

GUDID 00192896040960

HOUSE GELFOAM PRESS

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable

• Primary Device ID: 00192896040960
• NIH Device Record Key: f043d923-7279-4e02-88cd-1adba0123b9b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HOUSE GELFOAM PRESS
• Version Model Number: 468-531
• Catalog Number: 468-531
• 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: 6.125 Inch
• Length: 6.125 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896040960 [Primary]

FDA Product Code

• HWN: INSTRUMENT, COMPRESSION

Sterilization

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

[00192896040960]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-08-21
• Device Publish Date: 2018-09-11

On-Brand Devices [HOUSE GELFOAM PRESS]

• 00192896040991: HOUSE GELFOAM PRESS
• 00192896040960: HOUSE GELFOAM PRESS
• 00192896040953: HOUSE GELFOAM PRESS