FDA UDI In Commercial Distribution 🇺🇸 United States

RUSCH

DI: 14026704923486 · Model: IPN928865 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
RUSCH
Primary DI
14026704923486
Version / Model
IPN928865
Catalog Number
ECK105
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-16
Public Version
1
Public Version Date
2024-02-26
Public Version Status
New
Public Device Record Key
fdd649f0-a4ab-430c-9a84-e1b352158ef4

Device Description

10FR Female

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 34026704923480
Primary 14026704923486
Package 24026704923483

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K000070 000

Device Sizes

Type Value Unit Text
Height 1.2 Inch
Length 9.9 Inch
Width 5 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
false