Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

RIMPulse firmware — Class IIa MDD by Pulse for Integrated…

MD Atlas
Pulse for Integrated Solutions GmbH

EUDAMED last updated this device on Jul 31, 2024

RIMPulse firmware

B-04262384740088

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Pulse for Integrated Solutions GmbH
UDI-DI code: 04262384740088
Reference / catalog number: 4262384740088

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Pulse for Integrated Solutions GmbH
SRN: DE-MF-000024533
Manufacturer status: Active

Market distribution

Primary placement in XI; available across 1 country total.

Country	On market since	Until
XIPrimary placement		Still on market

Device identification

Trade name: RIMPulse firmware
UDI-DI code: 04262384740088
Basic UDI-DI: B-04262384740088
Reference / catalog number: 4262384740088
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12030601COMPLETE VITAL SIGNS TELEMETRY SYSTEMS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Related devices

RIMPulse Android Mobile ApplicationB-04262384740040On the market RIMPulse Android Watch applicationB-04262384740101On the market RIMPulse Apple Watch applicationB-04262384740064On the market RIMPulse iOS Mobile applicationB-04262384740057On the market RIMPulse Mobile ECG Device and SystemB-04262384740026On the market