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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

17150300001 — Class I MDR by Heinz Schiebler,…

MD Atlas
Heinz Schiebler, Norddeutsche Gummistrumpffabrik GmbH & Co. KG

EUDAMED last updated this device on Feb 8, 2022

17150300001

4053351KNEECAL6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Heinz Schiebler, Norddeutsche Gummistrumpffabrik GmbH & Co. KG
UDI-DI code: 04042372465342
Reference / catalog number: 17150300001

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Manufacturer information

Organization name: Heinz Schiebler, Norddeutsche Gummistrumpffabrik GmbH & Co. KG
SRN: DE-MF-000005267
Manufacturer status: Active

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: 04042372465342
Basic UDI-DI: 4053351KNEECAL6
Reference / catalog number: 17150300001
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)

Y061209KNEE ORTHOSES

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

This device is not currently linked to any other device.

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.