BOEHRINGER® ViSiGi 3D® Calibration System size 32Fr Bypass/Short w/bulb

GUDID 30816286020851

Gastric calibration tube, non-sterile

Primary Device ID	30816286020851
NIH Device Record Key	d3424f7c-5dae-4b77-aca2-5d36c1562ece
Commercial Distribution Status	In Commercial Distribution
Brand Name	BOEHRINGER® ViSiGi 3D® Calibration System size 32Fr Bypass/Short w/bulb
Version Model Number	5232SB
Company DUNS	079991657
Company Name	BOEHRINGER LABORATORIES, LLC
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	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	10816286020857 [Primary]
GS1	30816286020851 [Package] Contains: 10816286020857 Package: Box [5 Units] In Commercial Distribution
GS1	50816286020855 [Package] Contains: 10816286020857 Package: Carton [25 Units] In Commercial Distribution

KNT	Tubes, Gastrointestinal (And Accessories)

Steralize Prior To Use	false
Device Is Sterile	false

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Mark Image Registration \| Serial	Company Trademark Application Date
BOEHRINGER 97186870 not registered Live/Pending	Boehringer Laboratories, LLC 2021-12-23
BOEHRINGER 97186834 not registered Live/Pending	Boehringer Laboratories, LLC 2021-12-23
BOEHRINGER 79167386 not registered Dead/Abandoned	MAG IAS GmbH 2015-04-01
BOEHRINGER 79149890 4887150 Live/Registered	MAG IAS GmbH 2014-03-27
BOEHRINGER 78300425 2934276 Dead/Cancelled	Boehringer Ingelheim Pharma GmbH & Co. KG 2003-09-15
BOEHRINGER 77658159 3748503 Live/Registered	Boehringer Laboratories, Inc. 2009-01-28
BOEHRINGER 72457895 1365035 Live/Registered	BOEHRINGER, JOHN R. 1973-05-18