FDA UDI In Commercial Distribution 🇺🇸 United States

GUIDELINER

DI: 10841156100643 · Model: IPN913572 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GUIDELINER
Primary DI
10841156100643
Version / Model
IPN913572
Catalog Number
5573
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-01
Public Version
7
Public Version Date
2024-01-25
Public Version Status
Update
Public Device Record Key
7ca3eb96-753e-453f-9c82-205d09e2b16f

Device Description

GuideLiner V3 8F

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
No
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 30841156100647
Primary 10841156100643

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 8 French