FDA UDI In Commercial Distribution 🇺🇸 United States

RUSCH

DI: 04026704437214 · Model: IPN050001 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
RUSCH
Primary DI
04026704437214
Version / Model
IPN050001
Catalog Number
650704120
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-16
Public Version
9
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
09a345ae-680e-4b0b-871d-b6a2cdd7f271

Device Description

2 WAY 10ml PVC SUPRAPUBIC PUNCTURE INSTRUMENT, STERILE PACK

Device Characteristics

Single Use
Yes
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
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
KOB CATHETER, SUPRAPUBIC (AND ACCESSORIES)

GMDN Terms

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

Identifiers

Type ID
Package 44026704437212
Package 24026704437218
Primary 04026704437214

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K952187 000

Device Sizes

Type Value Unit Text
Length 206 Millimeter
Outer Diameter 4 Millimeter