FDA UDI In Commercial Distribution 🇺🇸 United States

LUTONIX® Drug Coated Balloon

DI: 00801741187803 · Model: LX351001260V · LUTONIX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUTONIX® Drug Coated Balloon
Primary DI
00801741187803
Version / Model
LX351001260V
Catalog Number
LX351001260V
Company Name
LUTONIX, INC.
Labeler DUNS
946734808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-31
Public Version
1
Public Version Date
2020-02-10
Public Version Status
New
Public Device Record Key
cc3133e2-538b-4118-9ce5-bf2a039e7ac3

Device Description

Lutonix 035 12X60MMX100CM

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
PRC Drug-coated peripheral transluminal angioplasty catheter

GMDN Terms

Code Name
62551 Peripheral angioplasty balloon catheter, drug-coated

Identifiers

Type ID
Primary 00801741187803

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Balloon Diameter, 12 Millimeter
Device Size Text, specify Catheter Length, 100 Centimeter
Device Size Text, specify Balloon Length, 60 Millimeter