Zvu® HRIM-201-12-KIT

GUDID 00816734022917

Zvu® HRiM Probe Kit

DIVERSATEK HEALTHCARE, INC.

Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system
Primary Device ID00816734022917
NIH Device Record Keye2fc552f-957d-48a0-aed8-29c0d2bac278
Commercial Distribution StatusIn Commercial Distribution
Brand NameZvu®
Version Model NumberHRIM-201-12-KIT
Catalog NumberHRIM-201-12-KIT
Company DUNS030650113
Company NameDIVERSATEK HEALTHCARE, INC.
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com

Device Dimensions

Catheter Gauge12 French
Catheter Gauge12 French
Catheter Gauge12 French
Catheter Gauge12 French
Catheter Gauge12 French
Catheter Gauge12 French
Catheter Gauge12 French
Catheter Gauge12 French

Device Identifiers

Device Issuing AgencyDevice ID
GS100816734022917 [Primary]
GS100816734022917 [Primary]
GS100816734022917 [Primary]
GS100816734022917 [Primary]
GS100816734022917 [Primary]
GS100816734022917 [Primary]
GS100816734022917 [Primary]
GS100816734022917 [Primary]

FDA Product Code

FFXSystem, Gastrointestinal Motility (Electrical)
FFXSystem, Gastrointestinal Motility (Electrical)
FFXSystem, Gastrointestinal Motility (Electrical)
FFXSystem, Gastrointestinal Motility (Electrical)
FFXSystem, Gastrointestinal Motility (Electrical)
FFXSystem, Gastrointestinal Motility (Electrical)
FFXSystem, Gastrointestinal Motility (Electrical)
FFXSystem, Gastrointestinal Motility (Electrical)

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00816734022917]

High-level Disinfectant


[00816734022917]

High-level Disinfectant


[00816734022917]

High-level Disinfectant


[00816734022917]

High-level Disinfectant


[00816734022917]

High-level Disinfectant


[00816734022917]

High-level Disinfectant


[00816734022917]

High-level Disinfectant


[00816734022917]

High-level Disinfectant


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-09
Device Publish Date2020-10-30

On-Brand Devices [Zvu®]

00816734022924Zvu® HRAM Starter Kit
00816734022917Zvu® HRiM Probe Kit
00816734022863Zvu® Anorectal Manometry Procedure Kit
00816734022856Zvu® Anorectal Balloons
00816734022740HRAM Protocol for BioView
00816734022733Zvu® HRAM Probe
00816734022689Zvu® HRiM Probe

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