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Amalgam Carriers Double Ended

EUDAMED

Class I (EU MDR)

Ref 3012Ref 3013Ref 3008

by Nadir & CO

Identity

Trade Name
Amalgam Carriers Double Ended EUDAMED
Device Name
Amalgam Carriers Double Ended EUDAMED
Model / Reference
3012 EUDAMED
3013 EUDAMED
3008 EUDAMED

Identifiers

Primary DI / UDI-DI
G15530120 EUDAMED
G15530130 EUDAMED
G15530080 EUDAMED
Basic UDI-DI
++G1553012YM EUDAMED
++G1553013YP EUDAMED
++G1553008YW EUDAMED
EMDN Code
Q010505 AMALGAM APPLICATORS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED
Austria 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

A comprehensive medical device directory listing for the Amalgam Carriers Double Ended device.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Nadir & CO
EUDAMED SRN
PK-MF-000026725
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (3)

  • EUDAMED 4c137b86-51be-4e44-be47-742a5050e86d 61 fields · synced Jul 30, 2026
  • EUDAMED f4d04206-7294-4c90-a73f-fc12e6ea273a 61 fields · synced May 18, 2026
  • EUDAMED d0c4943b-e5e4-4673-8ff3-16e1039a48d0 61 fields · synced May 18, 2026