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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

OS256/9 — Class I MDR by Ttape Company

MD Atlas
Ttape Company

EUDAMED last updated this device on May 29, 2026

OS256/9

871797315LTTP-002OTGV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ttape Company
UDI-DI code: 08717973151814
Reference / catalog number: OS256/9

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Manufacturer information

Organization name: Ttape Company
SRN: NL-MF-000003944
Manufacturer status: Active

Related devices

BNS202/S871797315LTTP-003OTH2On the market BC200W871797315LTTP-004OTH7On the market IB326871797315LTTP-005OTHC4QOn the market IB201/NS871797315LTTP-005OTHC4QOn the market IRB201871797315LTTP-005OTHC4QOn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	May 6, 1999	May 29, 2026

Device identification

Trade name: not provided
UDI-DI code: 08717973151814
Basic UDI-DI: 871797315LTTP-002OTGV
Reference / catalog number: OS256/9
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: Turbocast Ortho 60 x 90 cm x 2,5 mm - opti - skin
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M030504IMMOBILISATION SYSTEMS, MOULDABLE UNDER COLD AND HOT TEMPRATURES

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

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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.