FDA UDI Not in Commercial Distribution 🇺🇸 United States

TRUPUSH

DI: 10886704029168 · Model: 632-774X · Cerenovus, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRUPUSH
Primary DI
10886704029168
Version / Model
632-774X
Catalog Number
632774X
Company Name
Cerenovus, Inc.
Labeler DUNS
607846297
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-20
Public Version
5
Public Version Date
2023-09-15
Public Version Status
Update
Public Device Record Key
1b75d272-9335-48ec-a95d-ce76f3264bb1
Distribution End Date
2019-09-30

Device Description

TRUPUSH Coil Pusher 50 cm Coil Push Diameter .017 Inches (0.43 mm) Usable Length 195 cm

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
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
HCG DEVICE, NEUROVASCULAR EMBOLIZATION

GMDN Terms

Code Name
60940 Neurovascular embolization coil

Identifiers

Type ID
Primary 10886704029168

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071962 000