Impoaid 44019-001

GUDID 00850358007073

Battery Vacuum Erection Device

ENCORE, INC.

Penile vacuum device
Primary Device ID00850358007073
NIH Device Record Key1799b5d8-3441-4b32-be65-0f346f636c0d
Commercial Distribution StatusIn Commercial Distribution
Brand NameImpoaid
Version Model NumberVTU-E
Catalog Number44019-001
Company DUNS614647725
Company NameENCORE, INC.
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone800-475-3091
Emailinfo@revivepremium.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850358007073 [Primary]

FDA Product Code

LKYDevice, External Penile Rigidity

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-01

On-Brand Devices [Impoaid]

00850358007097Ring Kit
00850358007073Battery Vacuum Erection Device
00850358007004VTU-1

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.