FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Veraflo™

DI: 10849554014036 · Model: ULTVFL05SM · KCI USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
3M™ Veraflo™
Primary DI
10849554014036
Version / Model
ULTVFL05SM
Catalog Number
ULTVFL05SM
Company Name
KCI USA, INC.
Labeler DUNS
102726734
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-12
Public Version
1
Public Version Date
2023-07-20
Public Version Status
New
Public Device Record Key
1f6a601f-9bf9-459d-a634-be3020f930f3

Device Description

3M™ V.A.C. Veraflo™ Dressing, ULTVFL05SM, Small, Cavilon Warning Label, 5/CS

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OMP negative pressure wound therapy Powered suction pump

GMDN Terms

Code Name
61145 Irrigation negative-pressure wound therapy dressing

Identifiers

Type ID
Package 50849554014034
Primary 10849554014036

Customer Contacts