FDA UDI In Commercial Distribution 🇺🇸 United States

Cardiovascular Procedure Kit

DI: 00699753453395 · Model: 60018 · Terumo Cardiovascular Systems Corporation
Product Codes
0
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Cardiovascular Procedure Kit
Primary DI
00699753453395
Version / Model
60018
Company Name
Terumo Cardiovascular Systems Corporation
Labeler DUNS
177655466
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-17
Public Version
3
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
77b0c242-f75b-451a-b732-3946376c2bed

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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

GMDN Terms

Code Name
35441 Cardiopulmonary bypass system blood tubing set

Identifiers

Type ID
Package 50699753453390
Primary 00699753453395