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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

ME 3.200 — Class IIb MDD by Ultra-Controlo…

MD Atlas
Ultra-Controlo Projectos Industriais, Lda.

EUDAMED last updated this device on Feb 13, 2026

ME 3.200

B-05600347250691

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Ultra-Controlo Projectos Industriais, Lda.
UDI-DI code: 05600347250691
Reference / catalog number: ME 3.200

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View device family (Basic UDI)

Manufacturer information

Organization name: Ultra-Controlo Projectos Industriais, Lda.
SRN: PT-MF-000038820
Manufacturer status: Active

Related devices

SC 35-10B-05600347250660On the market SC 25-10B-05600347250226On the market SC 2-10B-05600347250004On the market SC 37-10B-05600347250981On the market ULTRAARB-05600347252275On 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05600347250691
Basic UDI-DI: B-05600347250691
Reference / catalog number: ME 3.200
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC 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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05600347250691

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z120309MEDICAL/MEDICINAL GAS PIPELINE SYSTEMS AND RELATED ACCESSORIES

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

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