Mespere

GUDID M9831104000031

Mespere LifeSciences Inc

Venous pressure monitor, invasive detection
Primary Device IDM9831104000031
NIH Device Record Key96884a7b-02fa-4ed4-acf5-347144b34a6c
Commercial Distribution StatusIn Commercial Distribution
Brand NameMespere
Version Model NumberMM-01
Company DUNS203147665
Company NameMespere LifeSciences Inc
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM9831104000031 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PFANon-Invasive Central Venous Manometer

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-05-06
Device Publish Date2016-10-06

On-Brand Devices [Mespere ]

M9831109000011OS-01
M9831108000031QG-V2000
M9831108000021IFU-V2000
M9831107000031SRA-V2000
M9831106000021IS-01
M9831105000061PS-01
M9831104000031MM-01
M9831104000021DS-01
M9831102000011DM-10
M9831101000041SEN-V2000

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