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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

APPLISIL — Class I MDR by UNION PLASTIC

MD Atlas
UNION PLASTIC

EUDAMED last updated this device on Dec 15, 2025

APPLISIL

3701225715ASVDU3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: UNION PLASTIC
UDI-DI code: 03701225740234
Reference / catalog number: 1ASV1137/1

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Manufacturer information

Organization name: UNION PLASTIC
SRN: FR-MF-000008940
Manufacturer status: Active

Related devices

APPLISIL3701225715ASVDU3On the market APPLISIL3701225715ASVFU7On the market APPLISIL3701225715ASVFU7On the market APPLISIL3701225715ASVFU7On the market APPLISIL3701225715ASVFU7On 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.

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: APPLISIL
UDI-DI code: 03701225740234
Basic UDI-DI: 3701225715ASVDU3
Reference / catalog number: 1ASV1137/1
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)

V0399MEASUREMENT DEVICES - 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
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Software identification