FDA UDI In Commercial Distribution 🇺🇸 United States

RUSCH

DI: 24026704550191 · Model: IPN053460 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
500

Basic Information

Brand Name
RUSCH
Primary DI
24026704550191
Version / Model
IPN053460
Catalog Number
A807
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
500
Record Status
Published
Publish Date
2018-09-15
Public Version
4
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
1a035ed8-62c4-45c8-a003-38dbfce314a2

Device Description

1" Foam Straps

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KGZ ACCESSORIES, CATHETER

GMDN Terms

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

Identifiers

Type ID
Primary 24026704550191
Unit of Use 14026704550194

Customer Contacts