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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

AA 150/14 — Class I MDR by nopa instruments…

MD Atlas
nopa instruments Medizintechnik GmbH

EUDAMED last updated this device on May 9, 2022

AA 150/14

404953800000004AQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: nopa instruments Medizintechnik GmbH
UDI-DI code: 14049538000864
Reference / catalog number: AA 150/14

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Manufacturer information

Organization name: nopa instruments Medizintechnik GmbH
SRN: DE-MF-000005613
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2000	Still on market

Device identification

Trade name: not provided
UDI-DI code: 14049538000864
Basic UDI-DI: 404953800000004AQ
Reference / catalog number: AA 150/14
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: HALSTED-MOSQUITO ART.FCPS STR 14,0 CM
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L0708010599SPECIFIC VESSELS CLAMPS, REUSABLE - 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

Related devices

AA 150/12404953800000004AQOn 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.