3.0 Liter Reservoir

GUDID 10896128002005

BELMONT INSTRUMENT CORPORATION

Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set Heat-exchanging intravenous administration set
Primary Device ID10896128002005
NIH Device Record Keya5d5e2ba-ccf0-444a-99e4-340d0861a8c6
Commercial Distribution StatusIn Commercial Distribution
Brand Name3.0 Liter Reservoir
Version Model Number903-00018
Company DUNS078330362
Company NameBELMONT INSTRUMENT CORPORATION
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110896128002005 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRNPump, Infusion

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-12-11
Device Publish Date2016-09-23

On-Brand Devices [3.0 Liter Reservoir]

10896128002005903-00018
00896128002008903-00018P

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