FDA UDI In Commercial Distribution 🇺🇸 United States

CuraFoam Foam Dressing

DI: 00616784301112 · Model: 3011 · DYNAREX CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
CuraFoam Foam Dressing
Primary DI
00616784301112
Version / Model
3011
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-21
Public Version
1
Public Version Date
2021-06-29
Public Version Status
New
Public Device Record Key
a8c9b13a-d78a-44fd-9f58-3e26795f5b8a

Device Description

CuraFoam Foam Dressing 2"x2"

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAC Dressing, Wound, Hydrophilic
NAD Dressing, Wound, Occlusive

GMDN Terms

Code Name
47407 Negative-pressure wound therapy system foam dressing, antimicrobial

Identifiers

Type ID
Package 00616784301129
Primary 00616784301112
Package 00616784301136