FDA UDI In Commercial Distribution 🇺🇸 United States

GOODWIN LUNG LINE

DI: B0664110100000 · Model: 411010-000 · NOVOSCI CORP.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
GOODWIN LUNG LINE
Primary DI
B0664110100000
Version / Model
411010-000
Catalog Number
411010-000
Company Name
NOVOSCI CORP.
Labeler DUNS
938289980
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-24
Public Version
2
Public Version Date
2023-07-07
Public Version Status
Update
Public Device Record Key
997a0878-935b-44de-bde9-0dacd01072ca

Device Description

A sterile device designed to facilitate/regulate the delivery of cardioplegic solution to the heart during a cardiopulmonary bypass procedure by connecting an administration line to a cardioplegia cannula. Also known as a cardioplegia delivery set, it basically consists of tubing [e.g., polyvinyl chloride (PVC)] with connectors. It may have a single lumen or branched multiple-lumen design and include various types of connectors, clamps, and valves, depending on additional intended uses (e.g., venting, recirculation, and/or simultaneous perfusion of vein grafts). This is a single-use device.

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
No
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
DTR Heat-Exchanger, Cardiopulmonary Bypass

GMDN Terms

Code Name
58824 Cardioplegia solution administration adaptor

Identifiers

Type ID
Primary B0664110100000
Package B0664110100003

Customer Contacts

Phone
800-854-0567

Premarket Submissions

Submission Number Supplement Number
K802545 000