FDA UDI In Commercial Distribution 🇺🇸 United States

TELEFLEX

DI: 10841156111649 · Model: IPN930693 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
TELEFLEX
Primary DI
10841156111649
Version / Model
IPN930693
Catalog Number
5888
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-13
Public Version
1
Public Version Date
2025-06-23
Public Version Status
New
Public Device Record Key
e7de0ce7-35a2-4e1d-9d0b-0a3c8d87b145

Device Description

Ringer Gen2, 4.0mm x 20mm, 1PK

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LOX Catheters, transluminal coronary angioplasty, percutaneous

GMDN Terms

Code Name
17521 Coronary angioplasty balloon catheter, perfusing

Identifiers

Type ID
Package 20841156111646
Primary 10841156111649
Package 30841156111643

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K233729 000