FDA UDI In Commercial Distribution 🇺🇸 United States

RUSCH

DI: 04026704022113 · Model: IPN050317 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
RUSCH
Primary DI
04026704022113
Version / Model
IPN050317
Catalog Number
173810-000200
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
9
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
468c0323-29ab-4f3f-9693-6a2a5c01d361

Device Description

Post OP 3 W Foley catheter,cyl.,2 eyes

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
EZL CATHETER, RETENTION TYPE, BALLOON

GMDN Terms

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

Identifiers

Type ID
Package 44026704022111
Package 24026704022117
Primary 04026704022113

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K972184 000

Device Sizes

Type Value Unit Text
Catheter Gauge 20 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry; Keep away from sunlight