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Organization name
UDI-DI code
Reference / catalog number

Stainless steel sterilization… — Class I MDR by FIMCO

MD Atlas
FIMCO

EUDAMED last updated this device on May 7, 2026

Stainless steel sterilization tray with silicone mat, 64 x 210 x 35 mm

3665857FAM0401P5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FIMCO
UDI-DI code: 03665857003078
Reference / catalog number: F2359A

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Manufacturer information

Organization name: FIMCO
SRN: FR-MF-000000175
Manufacturer status: Active

Related devices

Plastic sterilization tray with silicone mat, 160 x 70 x 20 mm3665857FAM0401P5On the market Plastic sterilization tray with silicone mat, 190 x 102 x 20 mm3665857FAM0401P5On the market Plastic sterilization tray with silicone mat, 250 x 150 x 20 mm3665857FAM0401P5On the market Plastic sterilization tray with silicone mat, 250 x 150 x 40 mm3665857FAM0401P5On the market Stainless steel sterilization tray with silicone mat, 127 x 210 x 35 mm3665857FAM0401P5On the market

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Feb 6, 2015	Still on market
Spain	May 12, 2025	Still on market

Device identification

Trade name: Stainless steel sterilization tray with silicone mat, 64 x 210 x 35 mm
UDI-DI code: 03665857003078
Basic UDI-DI: 3665857FAM0401P5
Reference / catalog number: F2359A
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)

V0499CLINICAL USE CONTAINERS (NON-IVD) - 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.