FDA UDI In Commercial Distribution 🇺🇸 United States

Impella

DI: 00813502012477 · Model: 1000200 · Abiomed, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Impella
Primary DI
00813502012477
Version / Model
1000200
Catalog Number
1000200
Company Name
Abiomed, Inc.
Labeler DUNS
050636737
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2023-06-19
Public Version
1
Public Version Date
2023-06-27
Public Version Status
New
Public Device Record Key
065e6ecd-abe9-43b5-9df1-d9518ba11f85

Device Description

Purge Cassette Gen02, 5-Packs

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
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
57791 Infusion pump cassette

Identifiers

Type ID
Unit of Use 00813502012460
Primary 00813502012477

Premarket Submissions

Submission Number Supplement Number
P140003 078
P170011 031