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Voss Coronary Bypass Vein Clamp

FDA UDI

Class II (US FDA UDI)

by Vm Cardio Vascular, Inc.

Identity

Trade Name
Voss Coronary Bypass Vein Clamp FDA UDI
Generic Name
Vascular clamp, single-use FDA UDI
Device Name
Coronary Bypass Vein Clamp (non-sterile) FDA UDI
Model / Reference
82931-NS FDA UDI
Description
Coronary Bypass Vein Clamp (non-sterile) FDA UDI

Identifiers

Primary DI / UDI-DI
00811304020089 FDA UDI
510(k) Number
K885161 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Vascular clamp, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Vascular clamp, single-use

Voss Coronary Bypass Vein Clamp by Vm Cardio Vascular, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular clamp, single-use.

Cleared under the same submission

K885161 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vm Cardio Vascular, Inc.

Sources (1)

  • FDA UDI e9e2888b-05e6-422a-b44d-a7d6d2b20caa 34 fields · synced May 30, 2026