FDA UDI In Commercial Distribution 🇺🇸 United States

Stellarex

DI: 00810060550304 · Model: AB35SX060040135-B · Philips Image Guided Therapy Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stellarex
Primary DI
00810060550304
Version / Model
AB35SX060040135-B
Catalog Number
AB35SX060040135
Company Name
Philips Image Guided Therapy Corporation
Labeler DUNS
118354223
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
2
Public Version Date
2023-08-17
Public Version Status
Update
Public Device Record Key
74772a19-a931-4483-814b-54176ab5ee90

Device Description

Stellarex 0.035 OTW Drug-coated Angioplasty Balloon (6mm x 40mm) x 135cm

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
Yes
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 00810060550304

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P160049 018

Device Sizes

Type Value Unit Text
Balloon Diameter 6 Millimeter
Balloon Length 40 Millimeter
Catheter Length 135 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight