Vaxaid VX-V7-D

GUDID 05060140208495

Vaxaid V7 Delux

DX PRODUCTS LIMITED

Penile vacuum device
Primary Device ID05060140208495
NIH Device Record Keyd6098009-9046-4aaa-b6e2-2a09f6c9c728
Commercial Distribution StatusIn Commercial Distribution
Brand NameVaxaid
Version Model NumberVaxaid V7 Delux
Catalog NumberVX-V7-D
Company DUNS216732051
Company NameDX PRODUCTS LIMITED
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 Usetrue
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

Customer Support Contacts

Phone+4401924288094
Emailtim@vaxaid.com

Device Dimensions

Lumen/Inner Diameter2.1 Inch
Depth7 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS105060140208488 [Primary]
GS105060140208495 [Package]
Contains: 05060140208488
Package: Box [10 Units]
In Commercial Distribution

FDA Product Code

LKYDevice, External Penile Rigidity

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-03-11
Device Publish Date2019-03-01

On-Brand Devices [Vaxaid]

05060140208532Vaxaid V9 Delux
05060140208518Vaxaid V7 Trainer
05060140208495Vaxaid V7 Delux
05060140208471Vaxaid V5 Trainer
05060140208457Vaxaid V5 Delux
05060140208419Vaxaid Peyronie's Disease

Trademark Results [Vaxaid]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VAXAID
VAXAID
79111275 4232045 Live/Registered
Ultramax Products Ltd
2012-03-27

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