Natus

GUDID 07290013818836

SLP INC

Electrode/transducer strap, reusable

• Primary Device ID: 07290013818836
• NIH Device Record Key: 570bd8ec-a1b3-4985-8e2d-3c4003faf787
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Natus
• Version Model Number: NA-1341
• Company DUNS: 023572393
• Company Name: SLP INC
• 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: false
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	07290013818836 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042253

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: 2016-09-20

On-Brand Devices [Natus]

• 07290013820167: NA-1475-Kit
• 07290013818843: NA-1550
• 07290013818836: NA-1341
• 07290013818829: NA-1340