FDA UDI In Commercial Distribution 🇺🇸 United States

MANIFOLD

DI: 00850004162019 · Model: VGAM0201 · VALFLUX GROUP, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MANIFOLD
Primary DI
00850004162019
Version / Model
VGAM0201
Catalog Number
VGAM0201
Company Name
VALFLUX GROUP, LLC
Labeler DUNS
050193715
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-19
Public Version
2
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
dd36b32d-6e04-4c38-933f-a2e03fb2f174

Device Description

VGAM0201 MANIFOLD

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DTL Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass

GMDN Terms

Code Name
47258 Contrast medium injection system administration set

Identifiers

Type ID
Primary 00850004162019

Customer Contacts