Pure Global

Vitatron Holding B.V. - Medical Device Manufacturer in United Kingdom

Vitatron Holding B.V. from Netherlands is a medical device manufacturer with 13 registered products in the UK MHRA database through Pure Global AI's free platform. The company produces 9 unique generic names across 2 device types.

This page provides comprehensive manufacturer intelligence including complete product portfolio and device type distribution. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify manufacturers, analyze portfolios, and discover partnership opportunities efficiently.

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13 Products
2 Types
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Vitatron Holding B.V.
Netherlands

Endepolsdomein 5

Maastricht, Netherlands

13
Total Products
9
Generic Names
2
Device Types
9
Generic Names
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Recent Registrations (13 most recent)
Most recently registered products with MHRA

Endocardial/interventricular septal pacing lead

Type:

General Medical Device

Device ID:

205962

Registration Date:

Dec 21, 2024

Dual-chamber implantable pacemaker, rate-responsive

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

71935

Registration Date:

Mar 26, 2021

Single-chamber implantable pacemaker, fixed-rate/demand

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

72004

Registration Date:

Mar 26, 2021

Cardiac pulse generator software

Type:

General Medical Device

Device ID:

168095

Registration Date:

Mar 26, 2021

Dual-chamber implantable pacemaker, demand

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

72002

Registration Date:

Mar 26, 2021

Endocardial pacing lead

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

71937

Registration Date:

Mar 26, 2021

Endocardial pacing lead

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

72001

Registration Date:

Mar 26, 2021

Single-chamber implantable pacemaker, fixed-rate/demand

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

71936

Registration Date:

Mar 26, 2021

Vascular catheter introduction set, nonimplantable

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

72005

Registration Date:

Mar 26, 2021

Cardiac pulse generator software

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

70664

Registration Date:

Mar 26, 2021

Implantable cardiac device management application software

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

72006

Registration Date:

Mar 26, 2021

Dual-chamber implantable pacemaker, rate-responsive

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

72003

Registration Date:

Mar 26, 2021

Single-chamber implantable pacemaker, rate-responsive

Type:

Active implantable device (Directive 90/385/EEC only)

Device ID:

71934

Registration Date:

Mar 26, 2021