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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

3501010118 — Class I MDR by Carpenter Engineered…

MD Atlas
Carpenter Engineered Foams Oy

EUDAMED last updated this device on Oct 21, 2024

3501010118

6438142FFC1AQV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Carpenter Engineered Foams Oy
UDI-DI code: 06438142101189
Reference / catalog number: 3501010118

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Manufacturer information

Organization name: Carpenter Engineered Foams Oy
SRN: FI-MF-000040986
Manufacturer status: Active

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35010100806438142FFC5AR9On the market 35010081626438142FFC1AQVOn the market 35010069596438142FFC1AQVOn the market 35010101176438142FFC1AQVOn the market 35010069216438142FFC5AR9On 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 Finland; available across 1 country total.

Placed on the market in Finland; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 06438142101189
Basic UDI-DI: 6438142FFC1AQV
Reference / catalog number: 3501010118
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)

V0899MEDICAL SUPPORT EQUIPMENT - 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