FDA UDI In Commercial Distribution 🇺🇸 United States

RUSCH

DI: 04026704543076 · Model: IPN052017 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
RUSCH
Primary DI
04026704543076
Version / Model
IPN052017
Catalog Number
346116
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
8
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
0b3671eb-bb45-4585-abd7-a9c851a2df3e

Device Description

Disposable

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
No
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
FBW FILIFORM AND FILIFORM FOLLOWER

GMDN Terms

Code Name
34917 Indwelling urethral drainage balloon catheter, non-antimicrobial

Identifiers

Type ID
Package 24026704543070
Primary 04026704543076
Package 44026704543074

Customer Contacts

Device Sizes

Type Value Unit Text
Length 19.5 Inch
Width 3 Inch
Height 0.31 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
false