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Harms-Colibri Forceps 0.12mm Titanium

EUDAMED

Class I (EU MDR)

Ref DT50-1520Model D50-1040-9990

by Daud Jee Mfg. Co

Identity

Trade Name
HARMS-COLIBRI FORCEPS 0.12MM TITANIUM EUDAMED
Device Name
Ophthalmic Forceps EUDAMED
Model / Reference
D50-1040-9990 EUDAMED
DT50-1520 EUDAMED

Identifiers

Primary DI / UDI-DI
+G006DT5015200W EUDAMED
Basic UDI-DI
++G006OphthalmicForceps9B EUDAMED
EMDN Code
L03130401 TISSUE AND ORGAN GRASPING FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Harms-Colibri Forceps 0.12mm Titanium by Daud Jee Mfg. Co — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Daud Jee Mfg. Co
EUDAMED SRN
PK-MF-000009615
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 589be973-ca7b-48a1-b570-d5e0f37dc220 61 fields · synced Jun 19, 2026