Patient Line Extension

GUDID 00896128002060

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
Primary Device ID00896128002060
NIH Device Record Keyad8102f6-0bfd-403e-a4fc-04819bd6ef10
Commercial Distribution StatusIn Commercial Distribution
Brand NamePatient Line Extension
Version Model Number903-00022P
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
GS100896128002060 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LGZWarmer, Thermal, Infusion Fluid

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 [Patient Line Extension]

10896128002067903-00022
00896128002060903-00022P

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