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Nucleus Expressor

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 6-630

by Duckworth & Kent Ltd.

Identity

Trade Name
Duckworth & Kent FDA UDI
Generic Name
Ophthalmic surgical probe, reusable FDA UDI
Device Name
Nucleus Expressor EUDAMEDFDA UDI
Model / Reference
6-630 EUDAMEDFDA UDI
Description
Nucleus Expressor FDA UDI

Identifiers

Catalog Number
6-630 FDA UDI
Primary DI / UDI-DI
05055313810247 EUDAMEDFDA UDI
Basic UDI-DI
B-05055313810247 EUDAMED
FDA Product Code
HNQ FDA UDI
EMDN Code
L1705 OPHTHALMOLOGY PROBES, 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

Nucleus Expressor 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 5f5415e8-da1c-4c11-a55f-a635afe9784b 61 fields · synced Jul 14, 2026
  • FDA UDI 994737d1-d06c-48ce-bc9f-7871d3733376 36 fields · synced May 29, 2026