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Organization name
UDI-DI code
Reference / catalog number

NICHROMINOX — Class I MDR by NICHROMINOX

MD Atlas
NICHROMINOX

EUDAMED last updated this device on Feb 23, 2026

NICHROMINOX

37014753SupRotInoxVW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NICHROMINOX
UDI-DI code: 03701475305337
Reference / catalog number: PN190210-4

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Manufacturer information

Organization name: NICHROMINOX
SRN: FR-MF-000000181
Manufacturer status: Active

Related devices

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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.

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: NICHROMINOX
UDI-DI code: 03701475305337
Basic UDI-DI: 37014753SupRotInoxVW
Reference / catalog number: PN190210-4
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: PLUG'IN 8 PERFO - VERT
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L15900699DENTAL MATERIAL PROCESSING INSTRUMENTS, 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

UDI-PI traceability

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