ri-integral flex flexible blade with integrated F. 12250

GUDID 04045396021686

The laryngoscopes are manufactured in order to be used for endotracheal intubation.

Rudolf Riester GmbH

Rigid intubation laryngoscope, reusable Rigid intubation laryngoscope, reusable Rigid intubation laryngoscope, reusable Rigid intubation laryngoscope, reusable Rigid intubation laryngoscope, reusable Rigid intubation laryngoscope, reusable Rigid intubation laryngoscope, reusable

• Primary Device ID: 04045396021686
• NIH Device Record Key: 7770c5a1-887b-4116-bee8-1e8b6bb65e17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ri-integral flex flexible blade with integrated F.
• Version Model Number: 12250
• Catalog Number: 12250
• Company DUNS: 537208717
• Company Name: Rudolf Riester GmbH
• 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: true
• 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	04045396021686 [Primary]

FDA Product Code

• CAL: Laryngoscope, Non-Rigid

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-07-27
• Device Publish Date: 2021-07-19

Devices Manufactured by Rudolf Riester GmbH

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