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

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Organization name
UDI-DI code
Reference / catalog number

2.3.6 — Class IIa MDR by Sherpa BV

MD Atlas
Sherpa BV

EUDAMED last updated this device on May 28, 2026

2.3.6

87202999688MSsherpaBZ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Sherpa BV
UDI-DI code: 87202999688132
Reference / catalog number: 2.3.6

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View device family (Basic UDI)

Manufacturer information

Organization name: Sherpa BV
SRN: NL-MF-000016928
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Oct 1, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 87202999688132
Basic UDI-DI: 87202999688MSsherpaBZ
Reference / catalog number: 2.3.6
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: MS sherpa is a digital solution for remote self-monitoring for persons with Multiple Sclerosis (MS) and their professional caregiver team(s), intended to support the monitoring of presence and progress of symptoms related to MS in order to provide personalized insights over time.
Additional information URL: https://www.mssherpa.nl/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)87202999688132

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

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Related devices

This device is not currently linked to any other device.

Certificates

Certificate health across this manufacturer's portfolio.

22M00170CRT01Issued
Quality management systemNotified body: 1912Expiry: Oct 1, 2030