FDA UDI In Commercial Distribution 🇺🇸 United States

CONNECTOR, 3/8" X 3/8" X 3/8" CLEAR PAY

DI: B066321333NS1 · Model: 321333NS · NOVOSCI CORP.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
500

Basic Information

Brand Name
CONNECTOR, 3/8" X 3/8" X 3/8" CLEAR PAY
Primary DI
B066321333NS1
Version / Model
321333NS
Catalog Number
321333NS
Company Name
NOVOSCI CORP.
Labeler DUNS
938289980
Distribution Status
In Commercial Distribution
Device Count in Pkg
500
Record Status
Published
Publish Date
2015-10-13
Public Version
3
Public Version Date
2023-07-13
Public Version Status
Update
Public Device Record Key
ee1484f5-6aa8-471e-8f1e-868e89575ea8

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

GMDN Terms

Code Name
64696 Non-ISO80369-standardized small-bore multichannel connector, single-use

Identifiers

Type ID
Package B066321333NS3
Primary B066321333NS1
Unit of Use B066321333NS0
Package B066321333NS4

Customer Contacts

Phone
800-854-0567

Premarket Submissions

Submission Number Supplement Number
K801404 000