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Hemopro, power cord, UK

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref VH-3012Model Vasoview Hemopro Power Cord

by Maquet Cardiovascular LLC

Identity

Trade Name
Vasoview Hemopro Power Cord EUDAMED
Hemopro, power cord, UK FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Hemopro, power cord, UK FDA UDI
Model / Reference
Vasoview Hemopro Power Cord EUDAMED
VH-3012 EUDAMED
C-VH-3012 FDA UDI
Description
Hemopro, power cord, UK FDA UDI

Identifiers

Catalog Number
C-VH-3012 FDA UDI
Primary DI / UDI-DI
00607567700840 EUDAMEDFDA UDI
Basic UDI-DI
0607567EVHCables2B EUDAMED
FDA Product Code
GEI FDA UDI
EMDN Code
K02010203 ELECTROSURGERY CONNECTION CABLES, SINGLE-USE EUDAMED
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical-only medical device connection cable, reusable

Hemopro, power cord, UK by Maquet Cardiovascular LLC — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI bef698f8-05c8-4676-b1e9-c41d10d6542f 35 fields · synced Jun 19, 2026
  • EUDAMED 724d9168-8379-4fb9-991b-a9fdb57c8e86 61 fields · synced Jun 19, 2026