FDA UDI In Commercial Distribution 🇺🇸 United States

Dermacea

DI: 50192253048672 · Model: 441102 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
96

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Dermacea
Primary DI
50192253048672
Version / Model
441102
Catalog Number
441102
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
96
Record Status
Published
Publish Date
2024-12-02
Public Version
1
Public Version Date
2024-12-10
Public Version Status
New
Public Device Record Key
f78c03ca-584a-46a5-b959-94cac6ae6756

Device Description

Dermacea Gauze Fluff Roll

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48127 Woven gauze roll/sheet

Identifiers

Type ID
Unit of Use 10192253048674
Primary 50192253048672

Device Sizes

Type Value Unit Text
Width 3.4 Inch
Length 3.6 Yard