3830 CC1845

GUDID 00817136026374

CCONN 1.375ID ORG X 15MM IDTPR

HANS RUDOLPH, INC.

Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph Pneumotachograph
Primary Device ID00817136026374
NIH Device Record Key0949be42-0ef2-4b37-befb-fb8d67dafef0
Commercial Distribution StatusIn Commercial Distribution
Brand Name3830
Version Model Number3830
Catalog NumberCC1845
Company DUNS007131725
Company NameHANS RUDOLPH, INC.
Device Count1
DM Exempttrue
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100817136026374 [Primary]

FDA Product Code

JAXPneumotachometer

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-30
Device Publish Date2020-11-20

On-Brand Devices [3830]

00817136026374CCONN 1.375ID ORG X 15MM IDTPR
008171360265413830 PNT LG FLG OD TPR W/FELUR

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