FDA UDI In Commercial Distribution 🇺🇸 United States

MediChoice

DI: 10885632127069 · Model: TD1004 · OWENS & MINOR DISTRIBUTION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MediChoice
Primary DI
10885632127069
Version / Model
TD1004
Company Name
OWENS & MINOR DISTRIBUTION, INC.
Labeler DUNS
007941230
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-21
Public Version
2
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
9b49c931-b6d1-4081-9497-693f36094174

Device Description

Dressing Wound Transparent Film 4 Inch X 4.75 Inch Sterile Not Made With Natural Rubber Latex MediChoice

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
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
KMK DEVICE, INTRAVASCULAR CATHETER SECUREMENT

GMDN Terms

Code Name
58301 Synthetic polymer semi-permeable film dressing, adhesive

Identifiers

Type ID
Package 30885632127063
Primary 10885632127069
Package 50885632127067