FDA UDI In Commercial Distribution 🇺🇸 United States

POD

DI: 00815948020320 · Model: 400POD3-A · PENUMBRA, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
POD
Primary DI
00815948020320
Version / Model
400POD3-A
Catalog Number
400POD3
Company Name
PENUMBRA, INC.
Labeler DUNS
191077671
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-15
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
0ad3cc2d-a75f-4b5f-90e8-441502534350

Device Description

POD Neuro, 3x20

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
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
HCG DEVICE, NEUROVASCULAR EMBOLIZATION

GMDN Terms

Code Name
43980 Embolization implant kit

Identifiers

Type ID
Primary 00815948020320

Premarket Submissions

Submission Number Supplement Number
K173614 000