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Lifescreen Pro Analyser, V1.x

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref LSPROModel Lifescreen Pro

by Spacelabs Healthcare Ltd

Identity

Trade Name
LIFESCREEN PRO ANALYSER, V1.X EUDAMED
Lifescreen Pro FDA UDI
Generic Name
Electrocardiographic long-term ambulatory recording analyser FDA UDI
Device Name
Lifescreen Pro EUDAMED
LIFESCREEN PRO ANALYSER, V1.X FDA UDI
Model / Reference
Lifescreen Pro EUDAMEDFDA UDI
LSPRO EUDAMED
Description
LIFESCREEN PRO ANALYSER, V1.X FDA UDI

Identifiers

Catalog Number
98800 FDA UDI
Primary DI / UDI-DI
10841522128837 EUDAMEDFDA UDI
Basic UDI-DI
08415221IIa98800OWNJN EUDAMED
FDA Product Code
DQK FDA UDI
EMDN Code
Z12050401 CARDIOVASCULAR HOLTER ANALYSERS EUDAMED
GMDN Term
Electrocardiographic long-term ambulatory recording analyser FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.1425 FDA UDI
Special Device Type
Software EUDAMED
Market of Registration
France 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Lifescreen Pro Analyser, V1.x by Spacelabs Healthcare Ltd — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
GB-MF-000001196
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED ecf16132-181e-41d6-8d0b-4583de49821f 61 fields · synced Jul 25, 2026
  • FDA UDI a40e14f5-0957-4b57-b8df-6d3f900b9b5b 34 fields · synced May 30, 2026