Trophon EPR

GUDID 09350855000139

Trophon US Refurbished

NANOSONICS LIMITED

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Primary Device ID09350855000139
NIH Device Record Key96ab12f0-86f4-4665-b211-dc9fb963204c
Commercial Distribution StatusIn Commercial Distribution
Brand NameTrophon EPR
Version Model NumberN00010-US-RFB
Company DUNS741021943
Company NameNANOSONICS LIMITED
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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS109350855000122 [Primary]
GS109350855000139 [Package]
Contains: 09350855000122
Package: [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OUJHigh Level Disinfection Reprocessing Instrument For Ultrasonic Transducers

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-09-09
Device Publish Date2016-09-21

On-Brand Devices [Trophon EPR]

09350855000139Trophon US Refurbished
09350855000115Trophon EPR Nth America AHECC 8419.20.00 (NNA VARIANT)
09350855000108Trophon EPR USA Variant AHECC 8419.20.00 (GE VARIANT)

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