Propper Miller Fiber Optic Laryngoscope Blade #0 19915600

GUDID 30818087011113

Propper Miller Fiber Optic Laryngoscope Blade #0

PROPPER MANUFACTURING COMPANY, INC.

Rigid intubation laryngoscope, reusable

• Primary Device ID: 30818087011113
• NIH Device Record Key: 3067a5ad-6466-4f49-ae69-26af4901e892
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Propper Miller Fiber Optic Laryngoscope Blade #0
• Version Model Number: 19915600
• Catalog Number: 19915600
• Company DUNS: 001483130
• Company Name: PROPPER MANUFACTURING COMPANY, 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	30818087011113 [Primary]

FDA Product Code

• CCW: Laryngoscope, Rigid

Sterilization

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

[30818087011113]

Ethylene Oxide;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-12
• Device Publish Date: 2020-03-04

On-Brand Devices [Propper Miller Fiber Optic Laryngoscope Blade #0]

• 30818087011434: Propper Miller Fiber Optic Laryngoscope Blade #0
• 30818087011113: Propper Miller Fiber Optic Laryngoscope Blade #0