SOMNO RESP accessory

GUDID 04250413410538

SOMNOmedics GmbH

Polysomnograph

• Primary Device ID: 04250413410538
• NIH Device Record Key: 0aad8152-e7ae-469b-9946-2fd5dd23bb65
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SOMNO RESP accessory
• Version Model Number: NGS302
• Company DUNS: 314112173
• Company Name: SOMNOmedics GmbH
• Device Count: 1
• DM Exempt: false
• 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: 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	04250413410538 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140861

FDA Product Code

• MNR: Ventilatory Effort Recorder

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-12-21

On-Brand Devices [SOMNO RESP accessory]

• 04250413410538: NGS302
• 04250413404643: TOS175
• 04250413404513: TOS170