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Vivo 1/2, Vivo 3

FDA UDI

Class II (US FDA UDI)

by Breas Medical, Inc.

Identity

Trade Name
Vivo 1/2, Vivo 3 FDA UDI
Generic Name
Electrical mains power cable FDA UDI
Device Name
Y Cable FDA UDI
Model / Reference
007006 FDA UDI
Description
Y Cable FDA UDI

Identifiers

Catalog Number
007006 FDA UDI
Primary DI / UDI-DI
07321820070060 FDA UDI
510(k) Number
K240778 FDA UDI
K240779 FDA UDI
FDA Product Code
MNS FDA UDI
MNT FDA UDI
GMDN Term
Electrical mains power cable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Category: Electrical mains power cable

Vivo 1/2, Vivo 3 by Breas Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical mains power cable.

Cleared under the same submission

K240778 also covers:

K240779 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Breas Medical, Inc.

Sources (1)

  • FDA UDI 0eaea782-e663-47cc-886d-7060d7452320 35 fields · synced Jun 8, 2026