PASHLEY LARYNGOSCOPE 1412-563

GUDID 00192896084360

PASHLEY LARYNGOSCOPE LASER ADULT SIZE

SONTEC INSTRUMENTS, INC.

Rigid intubation laryngoscope, reusable

• Primary Device ID: 00192896084360
• NIH Device Record Key: 5c331902-6f39-4904-a719-758b9475815e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PASHLEY LARYNGOSCOPE
• Version Model Number: 1412-563
• Catalog Number: 1412-563
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00192896084360 [Primary]

FDA Product Code

• CCW: LARYNGOSCOPE, RIGID

Sterilization

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

[00192896084360]

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: 2018-09-21

On-Brand Devices [PASHLEY LARYNGOSCOPE]

• 00192896084360: PASHLEY LARYNGOSCOPE LASER ADULT SIZE
• 00192896084353: PASHLEY LARYNGOSCOPE LASER SUPER PEDIATRIC SIZE