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DMEK Hook

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 6-250-2

by Duckworth & Kent Ltd.

Identity

Trade Name
Duckworth & Kent FDA UDI
Generic Name
Ophthalmic surgical probe, reusable FDA UDI
Device Name
DMEK Hook EUDAMEDFDA UDI
Model / Reference
6-250-2 EUDAMEDFDA UDI
Description
DMEK Hook FDA UDI

Identifiers

Catalog Number
6-250-2 FDA UDI
Primary DI / UDI-DI
05055313829669 EUDAMEDFDA UDI
Basic UDI-DI
B-05055313829669 EUDAMED
FDA Product Code
HNQ FDA UDI
EMDN Code
L1711 OPHTHALMOLOGY HOOKS, REUSABLE EUDAMED
GMDN Term
Ophthalmic surgical probe, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

DMEK Hook by Duckworth & Kent Ltd. — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
GB-MF-000002176
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED cd9048ea-ef40-49c0-9307-87ffc21d9326 61 fields · synced Oct 6, 2026
  • FDA UDI 1939fae0-0921-4288-807d-8ac2e3b3727f 36 fields · synced May 30, 2026