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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

Messschieber Townley Femur Caliper — Class IIa MDR

MD Atlas
Meditec Source GmbH & Co. KG

EUDAMED last updated this device on May 27, 2026

Messschieber Townley Femur Caliper

426246385PG169U

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Meditec Source GmbH & Co. KG
UDI-DI code: 04262463852176
Reference / catalog number: 1626-901

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View device family (Basic UDI)

Manufacturer information

Organization name: Meditec Source GmbH & Co. KG
SRN: DE-MF-000006490
Manufacturer status: Active

Related devices

2513-221426246385PG259VOn the market 2513-251426246385PG259VOn the market 2513-401426246385PG259VOn the market 2513-501426246385PG259VOn the market 0926-163426246385PG099XOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: Messschieber Townley Femur Caliper
UDI-DI code: 04262463852176
Basic UDI-DI: 426246385PG169U
Reference / catalog number: 1626-901
Issuing entity: GS1

Classification

Risk category: Class IIa
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04262463852176

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UDI-PI DataMatrix

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

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EMDN nomenclature code(s)

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

V0399MEASUREMENT DEVICES - 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

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