VAMP PLUS VP0753

GUDID 07460691955578

VAMP PLUS KIT - STERILE

Edwards Lifesciences LLC

Arterial blood sampling kit
Primary Device ID07460691955578
NIH Device Record Key2346f35b-aab0-4e24-9c39-6fa341e8cc2b
Commercial Distribution StatusIn Commercial Distribution
Brand NameVAMP PLUS
Version Model NumberVP0753
Catalog NumberVP0753
Company DUNS134139174
Company NameEdwards Lifesciences LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
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

Customer Support Contacts

Phone+1(800)822-9637
Emailtech_support@edwards.com

Device Dimensions

Length91 Inch

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *STORE IN A COOL, DRY PLACE.

Device Identifiers

Device Issuing AgencyDevice ID
GS107460691955578 [Primary]
GS157460691955573 [Package]
Package: Shipper [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KRACatheter, continuous flush

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-03

On-Brand Devices [VAMP PLUS]

07460691958616BLOOD MANAGEMENT SYSTEM
07460691955578VAMP PLUS KIT - STERILE
07460691944831BLOOD MANAGEMENT SYSTEM
07460691944824BLOOD MANAGEMENT SYSTEM.

Trademark Results [VAMP PLUS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VAMP PLUS
VAMP PLUS
75344794 2282031 Live/Registered
Edwards Lifesciences Corporation
1997-08-21

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