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KIT Quantum SuperPAC Tubing Set - 160R

FDA UDI

Class II (US FDA UDI)

by Spectrum Medical Limited

Identity

Trade Name
KIT Quantum SuperPAC Tubing Set - 160R FDA UDI
Generic Name
Cardiopulmonary bypass system blood tubing set FDA UDI
Model / Reference
SPC-160R FDA UDI

Identifiers

Primary DI / UDI-DI
28051160302530 FDA UDI
510(k) Number
K213540 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Cardiopulmonary bypass system blood tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4210 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiopulmonary bypass system blood tubing set

KIT Quantum SuperPAC Tubing Set - 160R by Spectrum Medical Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass system blood tubing set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 967e48b4-e528-4988-a9a1-7a776a8d9346 33 fields · synced May 30, 2026