FDA UDI In Commercial Distribution 🇺🇸 United States

RUSCH

DI: 44026704619113 · Model: IPN054394 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
RUSCH
Primary DI
44026704619113
Version / Model
IPN054394
Catalog Number
238300100
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-22
Public Version
5
Public Version Date
2024-01-10
Public Version Status
Update
Public Device Record Key
80058d52-e639-48aa-958e-1d8b76a26f10

Device Description

RUSCH GB: Female Catheter, Size 10 Fr 18cm

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
Yes
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
KOD CATHETER, UROLOGICAL

GMDN Terms

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

Identifiers

Type ID
Package 34026704619116
Package 14026704619112
Primary 44026704619113

Customer Contacts

Device Sizes

Type Value Unit Text
Length 18 Centimeter
Lumen/Inner Diameter 2.25 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
false