FDA UDI In Commercial Distribution 🇺🇸 United States

RUSCH

DI: 04026704055159 · Model: IPN052327 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
RUSCH
Primary DI
04026704055159
Version / Model
IPN052327
Catalog Number
410200-000160
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
4
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
3ff37232-12fb-4c53-888d-a47d54fe9d67

Device Description

Bladder catheter, Tiemann, 1 eye

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KOD CATHETER, UROLOGICAL

GMDN Terms

Code Name
42433 Intermittent urethral drainage catheter, non-antimicrobial, reusable

Identifiers

Type ID
Package 24026704055153
Primary 04026704055159
Package 44026704055157
Direct Marking 14026704055156

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 16 French