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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

Aprikos — Class I MDR by Aprikos Medical AS

MD Atlas
Aprikos Medical AS

EUDAMED last updated this device on May 15, 2026

Aprikos

7073371FILENO24X3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aprikos Medical AS
UDI-DI code: 07073371010421
Reference / catalog number: AM03-171-14

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View device family (Basic UDI)

Manufacturer information

Organization name: Aprikos Medical AS
SRN: NO-MF-000044411
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

HU25/00000077Issued
Quality assuranceNotified body: 1639Expiry: Aug 7, 2030

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Norway; available across 1 country total.

Country	On market since	Until
NorwayPrimary placement		Still on market

Device identification

Trade name: Aprikos
UDI-DI code: 07073371010421
Basic UDI-DI: 7073371FILENO24X3
Reference / catalog number: AM03-171-14
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: Tissue Forceps, 14,5 cm / 5 6 /8"
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)07073371010421

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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.

L031399GENERAL SURGERY FORCEPS, REUSABLE - 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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