Mespere

GUDID M9831106000021

Mespere LifeSciences Inc

Venous pressure monitor, invasive detection

• Primary Device ID: M9831106000021
• NIH Device Record Key: 612ddf98-579f-4d9c-b212-294b2bcfc66a
• Commercial Distribution Discontinuation: 2018-08-30
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Mespere
• Version Model Number: IS-01
• Company DUNS: 203147665
• Company Name: Mespere LifeSciences 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: true
• Serial Number: true
• Manufacturing Date: true
• 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
HIBCC	M9831106000021 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151776

FDA Product Code

• PFA: Non-Invasive Central Venous Manometer

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: 2020-05-06
• Device Publish Date: 2016-10-06

On-Brand Devices [Mespere ]

• M9831109000011: OS-01
• M9831108000031: QG-V2000
• M9831108000021: IFU-V2000
• M9831107000031: SRA-V2000
• M9831106000021: IS-01
• M9831105000061: PS-01
• M9831104000031: MM-01
• M9831104000021: DS-01
• M9831102000011: DM-10
• M9831101000041: SEN-V2000