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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

1805 — Class I MDR by True Tape Sports GmbH

MD Atlas
True Tape Sports GmbH

EUDAMED last updated this device on Jan 29, 2025

1805

PP0944218087

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: True Tape Sports GmbH
UDI-DI code: 111824943840
Reference / catalog number: 1805

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Manufacturer information

Organization name: True Tape Sports GmbH
SRN: DE-MF-000036380
Manufacturer status: Active

Related devices

1701PP0944217077On the market 1404PP0944214047On the market 1105PP0944210007On the market 1008PP0944210007On the market 1007PP0944210007On 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.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW032
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: 111824943840
Basic UDI-DI: PP0944218087
Reference / catalog number: 1805
Issuing entity: IFA

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 8
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)

M030402020103ELASTIC SUPPORT BANDAGES, COHESIVE, EXTENSIBLE IN TWO DIRECTIONS, HIGH EXTENSIBILITY

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