FDA UDI In Commercial Distribution 🇺🇸 United States

LP Coil System

DI: 00815948021990 · Model: RBYLP0104 · PENUMBRA, INC.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LP Coil System
Primary DI
00815948021990
Version / Model
RBYLP0104
Company Name
PENUMBRA, INC.
Labeler DUNS
191077671
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-21
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
4931aef8-b1da-4efc-b71b-0939868c7c84

Device Description

Ruby Coil LP, 1mm x 4cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
60941 Non-neurovascular embolization coil
60940 Neurovascular embolization coil

Identifiers

Type ID
Primary 00815948021990

Premarket Submissions

Submission Number Supplement Number
K192955 000