FDA UDI In Commercial Distribution 🇺🇸 United States

LUTONIX® Drug Coated Balloon

DI: 00801741163449 · Model: LX3513071005F · LUTONIX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUTONIX® Drug Coated Balloon
Primary DI
00801741163449
Version / Model
LX3513071005F
Catalog Number
LX3513071005F
Company Name
LUTONIX, INC.
Labeler DUNS
946734808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
4
Public Version Date
2024-01-09
Public Version Status
Update
Public Device Record Key
19c6243d-2f84-4ea4-b3ba-632b505981d8

Device Description

Lutonix 035 DCB, 7mm x 100mm x 130cm, 5F

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
ONU Drug-Eluting Peripheral Transluminal Angioplasty Catheter

GMDN Terms

Code Name
62551 Peripheral angioplasty balloon catheter, drug-coated

Identifiers

Type ID
Primary 00801741163449

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Catheter Length, 130 Centimeter
Device Size Text, specify Balloon Diameter, 7 Millimeter
Device Size Text, specify Balloon Length, 100 Millimeter