FDA UDI In Commercial Distribution 🇺🇸 United States

Penumbra Coil 400

DI: M4244002C14500 · Model: 4002C1450 · PENUMBRA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Penumbra Coil 400
Primary DI
M4244002C14500
Version / Model
4002C1450
Company Name
PENUMBRA, INC.
Labeler DUNS
191077671
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-30
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b5393de6-793f-4317-b298-23c48c999a2f

Device Description

PC400 Cplx Std, 14x50

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
43980 Embolization implant kit

Identifiers

Type ID
Primary M4244002C14500
Secondary 00814548010687

Premarket Submissions

Submission Number Supplement Number
K103305 000