FDA UDI In Commercial Distribution 🇺🇸 United States

Introcan Safety ® 2

DI: 04046955341955 · Model: 4232009-02 · B. BRAUN MEDICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Introcan Safety ® 2
Primary DI
04046955341955
Version / Model
4232009-02
Catalog Number
4232009-02
Company Name
B. BRAUN MEDICAL INC.
Labeler DUNS
002397347
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2022-03-25
Public Version
3
Public Version Date
2022-12-16
Public Version Status
Update
Public Device Record Key
03ee5e6f-129a-43be-a48c-1fddcc97db59

Device Description

Introcan Safety 2 - 20G x 1.25 in., PUR, Winged

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
MR Conditional
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
FOZ Catheter, intravascular, therapeutic, short-term less than 30 days

GMDN Terms

Code Name
32151 Peripheral vascular intervention infusion catheter

Identifiers

Type ID
Package 04046955341962
Primary 04046955341955
Unit of Use 04046955107360

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Catheter-Gauge : 20