FDA UDI In Commercial Distribution 🇺🇸 United States

Impella

DI: 00813502010985 · Model: 0042-0010-US · Abiomed, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Impella
Primary DI
00813502010985
Version / Model
0042-0010-US
Catalog Number
0042-0010-US
Company Name
Abiomed, Inc.
Labeler DUNS
050636737
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-08
Public Version
1
Public Version Date
2023-08-16
Public Version Status
New
Public Device Record Key
3908cd5c-e9c6-4a82-a562-6ea49c1959f0

Device Description

Impella Optical Controller, Packaged, US

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
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 00813502010985