FDA UDI In Commercial Distribution 🇺🇸 United States

B.BRAUN

DI: 04046955840854 · Model: 418024 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

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
B.BRAUN
Primary DI
04046955840854
Version / Model
418024
Catalog Number
418024
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2024-06-23
Public Version
1
Public Version Date
2024-07-01
Public Version Status
New
Public Device Record Key
6d83c783-df55-4d24-a706-394f24d1d51d

Device Description

IN2018 INTERMIT INJ PORT

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
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
41222 Medication transfer set

Identifiers

Type ID
Unit of Use 04046955840847
Primary 04046955840854

Customer Contacts