Flexible Video Rhino Laryngoscope M-205-22031-0101

GUDID B809M205220310101

Flexible Video Rhino Laryngoscope, diameter flexible end 2,9 mm

orlvision GmbH

Flexible video nasopharyngoscope

• Primary Device ID: B809M205220310101
• NIH Device Record Key: 0ef6f68c-4ac5-4ea4-80c2-034ce9fdc8da
• Commercial Distribution Discontinuation: 2025-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flexible Video Rhino Laryngoscope
• Version Model Number: RSX-P
• Catalog Number: M-205-22031-0101
• Company DUNS: 341467978
• Company Name: orlvision GmbH
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• 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: false
• Serial Number: true
• 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
HIBCC	B809M205220310101 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150248

FDA Product Code

• EQN: Laryngoscope, Nasopharyngoscope

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: 2020-03-16
• Device Publish Date: 2020-03-06

On-Brand Devices [Flexible Video Rhino Laryngoscope]

• B809M205240310101: Flexible Video Rhino Laryngoscope
• B809M205220310101: Flexible Video Rhino Laryngoscope, diameter flexible end 2,9 mm