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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

721250 — Class IIa MDR by Amann Girrbach AG

MD Atlas
Amann Girrbach AG

EUDAMED last updated this device on Jun 4, 2025

721250

++E494GIRFH6G

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Amann Girrbach AG
UDI-DI code: E4947212501
Reference / catalog number: 721250

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Manufacturer information

Organization name: Amann Girrbach AG
SRN: AT-MF-000000252
Manufacturer status: Active

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Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW018
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Austria; available across 2 countries total.

Country	On market since	Until
AustriaPrimary placement		Still on market
Germany		Still on market

Device identification

Trade name: not provided
UDI-DI code: E4947212501
Basic UDI-DI: ++E494GIRFH6G
Reference / catalog number: 721250
Issuing entity: HIBCC

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.

EMDN nomenclature code(s)

Q010601DENTAL ALLOYS

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.

G10 019612 0068Issued
Quality management systemNotified body: 0123Expiry: Jun 7, 2026