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Pulsenmore Ltd

Active in EUDAMED

Israelfrom SRN EUDAMED FDA SRN IL-MF-000037891 FEI 3020542149

Devices
7
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

Market reach

European Union
EUDAMED actor, 1 certificate
United States
FDA FEI

What Pulsenmore Ltd makes

Pulsenmore Ltd manufactures the Pulsenmore ES device, which is a Class IIa medical device.

The company is based in Israel and its devices are listed in the EUDAMED database.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

  • Pulsenmore FC Ref 400-0002

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Pulsenmore ES Ref 800-0013

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Pulsenmore ES Ref 400-0005

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa
  • Pulsenmore ES Ref 800-0011

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Pulsenmore ES Ref 800-0002

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Pulsenmore ES Ref 400-0003

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa
  • Pulsenmore ES Ref 400-0001

    Active Regimes: CE MDR De Novo Registry: EUDAMEDGUDID Class:IIa

Company details

EUDAMED SRN
IL-MF-000037891
FDA FEI number
3020542149
DUNS number
600380074
EUDAMED status
Active
EUDAMED registered name
Pulsenmore Ltd
EUDAMED abbreviated name
Pulsenmore
Registered address
8, omarim, 8496500, Omer, Israel
PRRC contact
Israel Citron(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 19 Aug 2030

EUDAMED certificates (1)

BSI Group The Netherlands B.V. 2797 1 certificate

  • MDR 811943 Active

    Quality management system EU MDR

    Issued
    20 Aug 2025
    Expires
    19 Aug 2030

Frequently asked questions

How many devices does PULSENMORE LTD have in the registry?

The registry currently lists 7 devices for PULSENMORE LTD. Devices recorded under merged duplicate company entries are counted once.

Which registries list PULSENMORE LTD's devices?

Among its 7 most recently registered devices, PULSENMORE LTD has devices listed in EUDAMED (7 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do PULSENMORE LTD's devices fall under?

Among its 7 most recently registered devices, the classes recorded for PULSENMORE LTD's devices are Class IIa. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for PULSENMORE LTD?

EUDAMED lists 1 certificate for PULSENMORE LTD (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 20 Aug 2025.

What are the newest devices from PULSENMORE LTD in the registry?

The most recently registered devices listed for PULSENMORE LTD include Pulsenmore FC and Pulsenmore ES.

Generated automatically from registry data and not verified by a human reviewer.