Pneupac

GUDID 30610586045749

SMITHS MEDICAL MD, INC.

Ventilator breathing circuit, single-use

• Primary Device ID: 30610586045749
• NIH Device Record Key: 523cfe7d-9602-4119-97aa-7277b5d2cdff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pneupac
• Version Model Number: WW122006
• Company DUNS: 106712748
• Company Name: SMITHS MEDICAL MD, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10610586045745 [Primary]
GS1	30610586045749 [Package]; Contains: 10610586045745; Package: BAG [15 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970158

FDA Product Code

• CBK: VENTILATOR, CONTINUOUS, FACILITY USE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-27
• Device Publish Date: 2015-09-01

On-Brand Devices [Pneupac]

• 30610586045749: WW122006
• 30610586045558: 124003
• 10610586045547: 123004
• 10610586045530: 123001
• 10610586045523: 123000
• 10610586045516: 122203
• 10610586045509: 122202
• 30610586038284: 122004