FDA UDI In Commercial Distribution 🇺🇸 United States

BOBBY/SOFIA Kit

DI: 00842429108574 · Model: SF6131-B895-US · Microvention, Inc.
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BOBBY/SOFIA Kit
Primary DI
00842429108574
Version / Model
SF6131-B895-US
Catalog Number
SF6131-B895
Company Name
Microvention, Inc.
Labeler DUNS
003263105
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-30
Public Version
2
Public Version Date
2026-04-28
Public Version Status
Update
Public Device Record Key
29611911-ea4f-4547-b134-cd722f965404

Device Description

BOBBY/SOFIA Kit

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
QJP Catheter, Percutaneous, Neurovasculature
DQO Catheter, intravascular, diagnostic
DQY Catheter, percutaneous

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use
32584 Intravascular occluding balloon catheter, image-guided

Identifiers

Type ID
Primary 00842429108574

Customer Contacts