EUDAMED last updated this device on Sep 2, 2026

Lastodur straff/strong

40495002057KB

On the marketClass I

Applicable legislation: —
Organization name: PAUL HARTMANN AG
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04049500225670
Reference / catalog number: 931629

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

Lastodur straff/strong is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by PAUL HARTMANN AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: Lastodur straff/strong
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04049500225670
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: 40495002057KB
Reference / catalog number: 931629
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: Class I
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: Long-stretch bandage
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 1400 MU10
10 MU10

Packaging levels

1 packaging level registered — each level carries its own UDI-DI.

04049500225670× 1 unitBase unit
- 04049500578783× 18 units

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04049500225670

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

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

M030402010101ELASTIC SUPPORT BANDAGES, NON-ADHESIVE, EXTENSIBLE IN ONE DIRECTION, HIGH EXTENSIBILITY

Critical warnings

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

Do not cut
CAUTION! Please note the additional information.
OTHER
Consult instructions for use

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Germany; available across 4 countries total.

Country	On market since	Until
GermanyPrimary placement	—	Still on market
Belgium	—	Still on market
Italy	—	Still on market
Slovenia	—	Still on market

Lastodur straff/strong

Device identification

Classification

Device details

Packaging levels

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Packaging levels

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Certificates covering this device

Related devices