FDA UDI In Commercial Distribution 🇺🇸 United States

Impella

DI: 00813502010022 · Model: 0042-0000-US · Abiomed, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Impella
Primary DI
00813502010022
Version / Model
0042-0000-US
Catalog Number
0042-0000-US
Company Name
Abiomed, Inc.
Labeler DUNS
050636737
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-21
Public Version
5
Public Version Date
2023-05-26
Public Version Status
Update
Public Device Record Key
30a7bf4c-1150-4d60-9faf-022ba58460ce

Device Description

Impella Controller, Packaged, US

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OZD Temporary Non-Roller Type Left Heart Support Blood Pump
PYX Temporary Non-Roller Type Right Heart Support Blood Pump

GMDN Terms

Code Name
57808 Intracardiac circulatory assist axial-pump catheter control unit

Identifiers

Type ID
Primary 00813502010022

Premarket Submissions

Submission Number Supplement Number
P140003 000
P170011 000