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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

MJK INSTRUMENTS — Class I MDR by MJK INSTRUMENTS

MD Atlas
MJK INSTRUMENTS

EUDAMED last updated this device on May 21, 2026

MJK INSTRUMENTS

3700998600001DENJ7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MJK INSTRUMENTS
UDI-DI code: 03700998600011
Reference / catalog number: IH001A

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Manufacturer information

Organization name: MJK INSTRUMENTS
SRN: FR-MF-000017000
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: MJK INSTRUMENTS
UDI-DI code: 03700998600011
Basic UDI-DI: 3700998600001DENJ7
Reference / catalog number: IH001A
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L010103HANDLES FOR SCALPELS, REUSABLE

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

Related devices

MJK INSTRUMENTS3700998600005DENK3On the market MJK INSTRUMENTS3700998600003DENJMOn the market MJK INSTRUMENTS3700998600003DENJMOn the market MJK INSTRUMENTS3700998600003DENJMOn the market MJK INSTRUMENTS3700998600003DENJMOn 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.