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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

101002 — Class I MDR by Hager & Werken GmbH &…

MD Atlas
Hager & Werken GmbH & Co. KG

EUDAMED last updated this device on Mar 2, 2026

101002

409963700010033

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Hager & Werken GmbH & Co. KG
UDI-DI code: 04099637002125
Reference / catalog number: 101002

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Manufacturer information

Organization name: Hager & Werken GmbH & Co. KG
SRN: DE-MF-000004938
Manufacturer status: Active

Related devices

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Market distribution

Primary placement in Germany; available across 3 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market
Luxembourg		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04099637002125
Basic UDI-DI: 409963700010033
Reference / catalog number: 101002
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)

Q010207DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY

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

Certificates

Certificate health across this manufacturer's portfolio.

HZ 1011605-1Issued
Quality management systemNotified body: 0197Expiry: May 21, 2031