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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

INSTANT-COMFORT-STD — Class I MDR by Mepholife

MD Atlas
Mepholife

EUDAMED last updated this device on Jul 24, 2025

INSTANT-COMFORT-STD

10032501INSTCOMFEW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mepholife
UDI-DI code: 08720892599124
Reference / catalog number: INSTANT-COMFORT-STD

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View device family (Basic UDI)

Manufacturer information

Organization name: Mepholife
SRN: NL-MF-000045921
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	Sep 1, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08720892599124
Basic UDI-DI: 10032501INSTCOMFEW
Reference / catalog number: INSTANT-COMFORT-STD
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Single-use, non-invasive acupressure patch designed to relieve headaches, reduce nasal congestion, and alleviate fatigue by stimulating specific acupoints on the face. The device is based on traditional acupuncture principles and does not contain active electronic components.
Additional information URL: No additional information URL provided by the manufacturer.
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)08720892599124

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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

FEMME-COMFORT-STD10032501FEMMCOMF3HOn the market Signature10032501SIGNATURERXOn the market

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.