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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

100014071 — Class I MDR by spektramed GmbH

MD Atlas
spektramed GmbH

EUDAMED last updated this device on Jul 18, 2022

100014071

425055662315044CB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: spektramed GmbH
UDI-DI code: 04250556606355
Reference / catalog number: 100014071

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Manufacturer information

Organization name: spektramed GmbH
SRN: DE-MF-000005711
Manufacturer status: Active

Related devices

100014072425055662315044CBOn the market 100014073425055662315044CBOn the market 100014070425055662315044CBOn the market 100023002/1425055662315040C3On the market 100023001/1425055662315040C3On 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

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

CW030
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW262
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04250556606355
Basic UDI-DI: 425055662315044CB
Reference / catalog number: 100014071
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: https://www.spektramed.de/produkte/rumpf/aktiv-spine
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y060399SPINE ORTHOSES - 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