FDA UDI In Commercial Distribution 🇺🇸 United States

TELEFLEX

DI: 14026704943255 · Model: 20096160 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
TELEFLEX
Primary DI
14026704943255
Version / Model
20096160
Catalog Number
20096160
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-10
Public Version
1
Public Version Date
2026-04-20
Public Version Status
New
Public Device Record Key
a64f71fc-1556-44bc-861f-834660f214fe

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GBM CATHETER, URETHRAL

GMDN Terms

Code Name
45603 Single-administration urethral drainage catheter

Identifiers

Type ID
Package 24026704943252
Primary 14026704943255

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183461 000

Device Sizes

Type Value Unit Text
Outer Diameter 5.3 Millimeter