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Organization name
UDI-DI code
Reference / catalog number

Single-use Lid Retractor… — Class IIa MDR by Fuhrmann GmbH

MD Atlas
Fuhrmann GmbH

EUDAMED last updated this device on Dec 15, 2025

Single-use Lid Retractor Desmarres, 12 mm x 160 mm, sterile

40548580252I1401JZ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Fuhrmann GmbH
UDI-DI code: 04054858302492
Reference / catalog number: 360017-3

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Manufacturer information

Organization name: Fuhrmann GmbH
SRN: DE-MF-000006652
Manufacturer status: Active

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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.

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

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

Device identification

Trade name: Single-use Lid Retractor Desmarres, 12 mm x 160 mm, sterile
UDI-DI code: 04054858302492
Basic UDI-DI: 40548580252I1401JZ
Reference / catalog number: 360017-3
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: 12 x 160 mm

EMDN nomenclature code(s)

V9012NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE

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