FDA UDI Not in Commercial Distribution 🇺🇸 United States

ION™

DI: 08714729810698 · Model: H7493902428350 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
ION™
Primary DI
08714729810698
Version / Model
H7493902428350
Catalog Number
H7493902428350
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
021717889
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
5
Public Version Date
2025-03-14
Public Version Status
Update
Public Device Record Key
ecc160b9-e569-43dd-a3a1-685b4c0b37ea
Distribution End Date
2016-12-06

Device Description

Paclitaxel-Eluting Platinum Chromium Coronary Stent System

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
MR Conditional
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
NIQ Coronary drug-eluting stent

GMDN Terms

Code Name
56284 Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated

Identifiers

Type ID
Primary 08714729810698

Device Sizes

Type Value Unit Text
Device Size Text, specify 28 mm Stent Length
Device Size Text, specify 3.5 mm Stent Diameter