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Vessel Cannula, 3mm

FDA UDI

Class II (US FDA UDI)

by Quest Medical Inc

Identity

Trade Name
Vessel Cannula, 3mm FDA UDI
Generic Name
Vascular irrigation cannula, cardiac vessel graft FDA UDI
Model / Reference
VCC-03 FDA UDI

Identifiers

Catalog Number
VCC-03 FDA UDI
Primary DI / UDI-DI
20634624533039 FDA UDI
510(k) Number
K971928 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Vascular irrigation cannula, cardiac vessel graft 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

No

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

Yes

FDA UDI

Category: Vascular irrigation cannula, cardiac vessel graft

Vessel Cannula, 3mm by Quest Medical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular irrigation cannula, cardiac vessel graft.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quest Medical Inc

Sources (1)

  • FDA UDI 61f53f5a-f515-4d44-bcd8-0bb9db348799 34 fields · synced May 30, 2026