LEMPERT RONGEUR 315-542

GUDID 00192896027374

LEMPERT RONGEUR STRAIGHT JAW

SONTEC INSTRUMENTS, INC.

Orthopaedic joint/limb rongeur

• Primary Device ID: 00192896027374
• NIH Device Record Key: c3f69dbb-ea86-42eb-8b9d-5e21d2926c92
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LEMPERT RONGEUR
• Version Model Number: 315-542
• Catalog Number: 315-542
• 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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896027374 [Primary]

FDA Product Code

• HTX: RONGEUR

Sterilization

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

[00192896027374]

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: 2019-07-12
• Device Publish Date: 2018-09-11

On-Brand Devices [LEMPERT RONGEUR]

• 00192896088573: LEMPERT RONGEUR STRAIGHT JAW
• 00192896088283: LEMPERT RONGEUR CURVED JAW
• 00192896048058: LEMPERT RONGEUR CURVED TIP
• 00192896027404: LEMPERT RONGEUR CURVED JAW
• 00192896027398: LEMPERT RONGEUR STRAIGHT JAW
• 00192896027381: LEMPERT RONGEUR CURVED JAW
• 00192896027374: LEMPERT RONGEUR STRAIGHT JAW
• 00192896095908: CLASSIC LEMPERT RONGEUR STRAIGHT TIP