Laryngoscope Blades

GUDID 00616784402819

Laryngoscope Blades Disposable Fiber Optic Sterile

DYNAREX CORPORATION

Laryngoscope blade, single-use Laryngoscope blade, single-use Laryngoscope blade, single-use Laryngoscope blade, single-use

• Primary Device ID: 00616784402819
• NIH Device Record Key: 27887225-be0a-45f6-8a04-9a3d54e52e6f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Laryngoscope Blades
• Version Model Number: 4028
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 10
• 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: true
• Lot Batch: false
• 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	00616784402819 [Unit of Use]
GS1	00616784402826 [Primary]
GS1	00616784402833 [Package]; Contains: 00616784402826; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• CCW: Laryngoscope, Rigid

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-11-10
• Device Publish Date: 2020-11-02

On-Brand Devices [Laryngoscope Blades]

• 00616784402819: Laryngoscope Blades Disposable Fiber Optic Sterile
• 00616784402710: Laryngoscope Blades Disposable Fiber Optic Sterile
• 00616784402611: Laryngoscope Blades Disposable Fiber Optic Sterile
• 00616784402512: Laryngoscope Blades Disposable Fiber Optic Sterile
• 00616784402413: Laryngoscope Blades Disposable - Fiber Optic Sterile