LUKENS THYMUS RETRACTOR 502-410

GUDID 00192896092334

LUKENS THYMUS RETRACTOR BLUE ELECTRO COATED

SONTEC INSTRUMENTS, INC.

ENT elevator

• Primary Device ID: 00192896092334
• NIH Device Record Key: 9c4af8bf-9b80-44a2-bfda-c3522af2de0e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUKENS THYMUS RETRACTOR
• Version Model Number: 502-410
• Catalog Number: 502-410
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 7 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896092334 [Primary]

FDA Product Code

• KAL: Retractor, Ent

Sterilization

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

[00192896092334]

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: 2019-07-12
• Device Publish Date: 2019-01-04

On-Brand Devices [LUKENS THYMUS RETRACTOR]

• 00192896092334: LUKENS THYMUS RETRACTOR BLUE ELECTRO COATED
• 00192896044227: LUKENS THYMUS RETRACTOR