FDA UDI In Commercial Distribution 🇺🇸 United States

GUIDELINER

DI: 10841156103804 · Model: IPN931265 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GUIDELINER
Primary DI
10841156103804
Version / Model
IPN931265
Catalog Number
5569
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-24
Public Version
1
Public Version Date
2025-11-03
Public Version Status
New
Public Device Record Key
a4a3bf55-743b-4d79-9db7-e019f213a6f2

Device Description

GuideLiner V3 catheter 5F

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
DQY Catheter, percutaneous

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Package 20841156103801
Primary 10841156103804
Package 30841156103808

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 5 French