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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

ATMOS C 261 Aspirator / Receptal®… — Class IIa MDD

MD Atlas
ATMOS MedizinTechnik GmbH & Co. KG

EUDAMED last updated this device on Mar 5, 2025

ATMOS C 261 Aspirator / Receptal® 1.5 l

B-04250365177411

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ATMOS MedizinTechnik GmbH & Co. KG
UDI-DI code: 04250365177411
Reference / catalog number: 313.0165.0

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Manufacturer information

Organization name: ATMOS MedizinTechnik GmbH & Co. KG
SRN: DE-MF-000005570
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
See chapter 2.0 " Notices for your safety" in the valid instructions for use of the product.
CW999
Medical contra-indications: Not suitable for:  continuous operation in cases of drainage in the low-vacuum range (e.g., cardiothoracic drainage or wound drainage)  permanent endoscopic use  vacuum extraction  smoke evacuation  liposuction  emergency or rescue operation Other contra-indications: Not suitable for:  suctioning outdoors / during transport  suction of flammable, corrosive, and explosive substances  suction in potentially explosive atmospheres

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: ATMOS C 261 Aspirator / Receptal® 1.5 l
UDI-DI code: 04250365177411
Basic UDI-DI: B-04250365177411
Reference / catalog number: 313.0165.0
Issuing entity: GS1

Classification

Risk category: Class IIa
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.

EMDN nomenclature code(s)

Z120105SURGICAL MEDICAL ASPIRATORS

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

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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.