FDA UDI In Commercial Distribution 🇺🇸 United States

Interlock™

DI: 08714729845300 · Model: M001361940 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Interlock™
Primary DI
08714729845300
Version / Model
M001361940
Catalog Number
M001361940
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
021717889
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
f7f756a6-9bbe-4179-a566-35e6e02ce2b2

Device Description

Fibered IDC™ Occlusion System

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
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
KRD Device, Vascular, for Promoting Embolization

GMDN Terms

Code Name
60941 Non-neurovascular embolization coil

Identifiers

Type ID
Primary 08714729845300

Device Sizes

Type Value Unit Text
Device Size Text, specify 50 cm Length
Device Size Text, specify 18 mm Diameter