DSI

GUDID 07290013820365

S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD

Polysomnography analyser

• Primary Device ID: 07290013820365
• NIH Device Record Key: f86e5748-fdc7-4687-b74b-6f98185a4cf8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DSI
• Version Model Number: 9101DSI
• Company DUNS: 600632715
• Company Name: S. L. P. SCIENTIFIC LABORATORY PRODUCTS LTD
• 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: true
• 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	07290013820365 [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 [DSI]

• 07290013820471: 9102DSI
• 07290013820365: 9101DSI
• 07290013820259: PS055-P-C
• 07290013820242: PS055-P-A
• 07290013820235: PS015-C-C
• 07290013820228: PS015-C-A
• 07290013820105: 9002-L30
• 07290013820099: 9002-L20