FDA UDI In Commercial Distribution 🇺🇸 United States

Penumbra Coil 400

DI: 00815948024953 · Model: 400PAC6 · PENUMBRA, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Penumbra Coil 400
Primary DI
00815948024953
Version / Model
400PAC6
Catalog Number
400PAC6
Company Name
PENUMBRA, INC.
Labeler DUNS
191077671
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-07
Public Version
1
Public Version Date
2023-03-15
Public Version Status
New
Public Device Record Key
7931ebc6-b247-443b-8a07-3bc2f11e6625

Device Description

PAC400, 6 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
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
60940 Neurovascular embolization coil
60941 Non-neurovascular embolization coil

Identifiers

Type ID
Primary 00815948024953

Premarket Submissions

Submission Number Supplement Number
K173614 000