FDA UDI In Commercial Distribution 🇺🇸 United States

Expo™

DI: 08714729523376 · Model: H749087383021 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Expo™
Primary DI
08714729523376
Version / Model
H749087383021
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
021717889
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
94f75ab6-9f0a-424f-8100-feaae9bbd9b5

Device Description

Angiographic Catheter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
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
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Package 08714729169338
Primary 08714729523376

Device Sizes

Type Value Unit Text
Device Size Text, specify 7 F Diameter
Device Size Text, specify 2.4 mm Diameter