FDA UDI In Commercial Distribution 🇺🇸 United States

MediChoice

DI: 10885632401312 · Model: 50010 · OWENS & MINOR DISTRIBUTION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MediChoice
Primary DI
10885632401312
Version / Model
50010
Company Name
OWENS & MINOR DISTRIBUTION, INC.
Labeler DUNS
007941230
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-15
Public Version
1
Public Version Date
2023-11-23
Public Version Status
New
Public Device Record Key
7d5d93e3-c078-41db-b0c2-b7b1990368a6

Device Description

Blood Transfer Device Male Luer Lock Connector Standard Polypropylene Transparent Single Use CA/800 Not made with Natural Rubber Latex MediChoice

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JKA Tubes, vials, systems, serum separators, blood collection

GMDN Terms

Code Name
35209 Non-fixed blood collection needle

Identifiers

Type ID
Package 30885632401316
Primary 10885632401312
Package 20885632401319

Premarket Submissions

Submission Number Supplement Number
K200027 000