FDA UDI In Commercial Distribution 🇺🇸 United States

Rem Systems

DI: 10813153026554 · Model: BC 2151 · CODAN US CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Rem Systems
Primary DI
10813153026554
Version / Model
BC 2151
Company Name
CODAN US CORPORATION
Labeler DUNS
058027475
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-31
Public Version
1
Public Version Date
2021-04-08
Public Version Status
New
Public Device Record Key
5000e8e3-1fbf-4f73-a14e-dafab0362ddd

Device Description

Extension Set with Ultra-Clear Valve

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 00813153026557
Primary 10813153026554