FDA UDI In Commercial Distribution 🇺🇸 United States

LUTONIX® Drug Coated Balloon

DI: 00801741177484 · Model: LX1810071505F · LUTONIX, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
LUTONIX® Drug Coated Balloon
Primary DI
00801741177484
Version / Model
LX1810071505F
Catalog Number
LX1810071505F
Company Name
LUTONIX, INC.
Labeler DUNS
946734808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-30
Public Version
4
Public Version Date
2026-04-27
Public Version Status
Update
Public Device Record Key
20b5c6c0-9a21-4779-8873-d15ba3b5895d

Device Description

Lutonix 018 7X150MMX100CM

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
Yes
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
ONU Drug-Eluting Peripheral Transluminal Angioplasty Catheter

GMDN Terms

Code Name
62551 Peripheral angioplasty balloon catheter, drug-coated

Identifiers

Type ID
Primary 00801741177484

Customer Contacts

Device Sizes

Type Value Unit Text
Balloon Length 150 Millimeter
Length 100 Centimeter
Device Size Text, specify Diameter = 7 millimetre (mm)

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep dry