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Weitlaner

EUDAMED

Class I (EU MDR)

Ref 06-750-13-07

by FHQ Trading CO.

Identity

Trade Name
Weitlaner EUDAMED
Device Name
Weitlaner EUDAMED
Model / Reference
06-750-13-07 EUDAMED

Identifiers

Primary DI / UDI-DI
G4380675013070 EUDAMED
Basic UDI-DI
++G438067501307F4 EUDAMED
EMDN Code
L03140199 SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Hand-held surgical retractor, reusable

Weitlaner by FHQ Trading CO. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
FHQ Trading CO.
EUDAMED SRN
PK-MF-000033179
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 7d1179c1-81fc-43f5-b125-42b384775759 61 fields · synced Jun 17, 2026