EXTENSION SET

GUDID 10810080610344

MPS Pharma & Medical, Inc.

Intravenous administration tubing extension set

• Primary Device ID: 10810080610344
• NIH Device Record Key: 1f6c7c0d-c09f-488a-bd4a-a991a4bd3fcb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EXTENSION SET
• Version Model Number: EB-072-03
• Company DUNS: 117970217
• Company Name: MPS Pharma & Medical, 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810080610347 [Primary]
GS1	10810080610344 [Package]; Contains: 00810080610347; Package: Case [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K955896

FDA Product Code

• LHI: Set, I.V. Fluid Transfer

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-01
• Device Publish Date: 2022-08-24

On-Brand Devices [EXTENSION SET]

• 10810080611662: EA-060-01
• 10810080610412: EI-060-02
• 10810080610405: EG-060-01
• 10810080610399: EG-014-01
• 10810080610382: ED-030-01
• 10810080610375: EC-072-01
• 10810080610368: EC-060-01
• 10810080610351: EB-096-01
• 10810080610344: EB-072-03
• 10810080610337: EB-072-02
• 10810080610313: EB-060-03
• 10810080610306: EB-060-02
• 10810080610290: EB-060-01
• 10810080610276: EB-038-11
• 10810080610252: EB-030-13
• 10810080610245: EB-030-02
• 10810080610238: EB-012-01
• 10810080610221: DB-006-05