BE 150-5G Test Lung BE 150-5G

GUDID M996BE1505G0

BE 150-5G Test Lung has a 22mm I.D. connection and a 1 liter capacity; Not made with natural rubber latex. Not for patient use.

INSTRUMENTATION INDUSTRIES, INCORPORATED

Lung physical simulator
Primary Device IDM996BE1505G0
NIH Device Record Key8f6b3804-baee-4a3c-ac12-22875efef175
Commercial Distribution StatusIn Commercial Distribution
Brand NameBE 150-5G Test Lung
Version Model NumberBE 150-5G
Catalog NumberBE 150-5G
Company DUNS053146767
Company NameINSTRUMENTATION INDUSTRIES, INCORPORATED
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone412-854-1133
Emailraqa@iiimedical.com
Phone412-854-1133
Emailraqa@iiimedical.com
Phone412-854-1133
Emailraqa@iiimedical.com
Phone412-854-1133
Emailraqa@iiimedical.com
Phone412-854-1133
Emailraqa@iiimedical.com
Phone412-854-1133
Emailraqa@iiimedical.com
Phone412-854-1133
Emailraqa@iiimedical.com
Phone412-854-1133
Emailraqa@iiimedical.com
Phone412-854-1133
Emailraqa@iiimedical.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM996BE1505G0 [Primary]
HIBCCM996BE1505G1 [Package]
Package: Ziplock poly bag [5 Units]
In Commercial Distribution

FDA Product Code

BTCBag, Reservoir

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-08-24
Device Publish Date2016-12-30

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