FDA UDI In Commercial Distribution 🇺🇸 United States

IODOSORB

DI: 05000223497385 · Model: 6602124014 · SMITH & NEPHEW MEDICAL LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
IODOSORB
Primary DI
05000223497385
Version / Model
6602124014
Catalog Number
6602124014
Company Name
SMITH & NEPHEW MEDICAL LIMITED
Labeler DUNS
216344051
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-31
Public Version
2
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
55952a40-e0d8-4760-9472-199e52aafebe

Device Description

Cadexomer iodine gel. 10g. Ctn of 1 Tube

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRO Dressing, Wound, Drug

GMDN Terms

Code Name
47474 Exudate-absorbent dressing, hydrophilic-gel, antimicrobial

Identifiers

Type ID
Package 00040565122564
Primary 05000223497385
Package 30040565122565
Package 05000223497392