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3/8" Coronary Perfusion Plug

FDA UDI

Class II (US FDA UDI)

by Novosci Corp.

Identity

Trade Name
3/8" CORONARY PERFUSION PLUG FDA UDI
Generic Name
Stopcock FDA UDI
Device Name
3/8" TUBING TO FIT OVER THE CORONARY PERFUSION OUTLET PORT OF AN OXYGENATOR, TO SECURELY SEAL OFF THE PORT, THUS REDUCING THE POSSIBLITY OF THE PORT BEING INADVERTENTLY OPENED DUTING THE HEMOPERFUSION PROCEEDURE. FDA UDI
Model / Reference
201022-000 FDA UDI
Description
3/8" TUBING TO FIT OVER THE CORONARY PERFUSION OUTLET PORT OF AN OXYGENATOR, TO SECURELY SEAL OFF THE PORT, THUS REDUCING THE POSSIBLITY OF THE PORT BEING INADVERTENTLY OPENED DUTING THE HEMOPERFUSION PROCEEDURE. FDA UDI

Identifiers

Catalog Number
201022-000 FDA UDI
Primary DI / UDI-DI
B0662010220000 FDA UDI
FDA Product Code
DTL FDA UDI
DWF FDA UDI
GMDN Term
Stopcock FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4290 FDA UDI
870.4210 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

3/8" Coronary Perfusion Plug by Novosci Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novosci Corp.

Sources (1)

  • FDA UDI e7236dc3-4967-446f-be29-4f68cea73a2f 35 fields · synced May 31, 2026