← Back to catalogue

HemoPro Power Supply

FDA UDI

Class II (US FDA UDI)

by Maquet Cardiovascular LLC

Identity

Trade Name
HemoPro Power Supply FDA UDI
Generic Name
Basic power supply, reusable FDA UDI
Device Name
Hemopro Power Supply FDA UDI
Model / Reference
C-VH-3010 FDA UDI
Description
Hemopro Power Supply FDA UDI

Identifiers

Catalog Number
VH-3010 FDA UDI
Primary DI / UDI-DI
00607567700826 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Basic power supply, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic power supply, reusable

HemoPro Power Supply by Maquet Cardiovascular LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic power supply, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1f73eb3c-f64b-4bc9-803c-c4059dd6c319 35 fields · synced May 30, 2026