TROUSSEAU TRACHEAL DILATOR RETRACTOR 502-382

GUDID 00192896044180

TROUSSEAU TRACHEAL DILATOR RETRACTOR PEDIATRIC SMALL SHAFT

SONTEC INSTRUMENTS, INC.

Tracheal surgery dilator, reusable

• Primary Device ID: 00192896044180
• NIH Device Record Key: b11d72d0-6da6-42bf-afaa-e1d197f7581a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TROUSSEAU TRACHEAL DILATOR RETRACTOR
• Version Model Number: 502-382
• Catalog Number: 502-382
• 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: 5.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896044180 [Primary]

FDA Product Code

• KCG: DILATOR, TRACHEAL

Sterilization

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

[00192896044180]

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: 2018-11-22
• Device Publish Date: 2018-09-14

On-Brand Devices [TROUSSEAU TRACHEAL DILATOR RETRACTOR]

• 00192896044197: TROUSSEAU TRACHEAL DILATOR RETRACTOR ADULT LARGE SHAFT
• 00192896044180: TROUSSEAU TRACHEAL DILATOR RETRACTOR PEDIATRIC SMALL SHAFT
• 00192896044173: TROUSSEAU TRACHEAL DILATOR RETRACTOR ADOLESCENT MEDIUM SHAFT