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Speculum

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9-579

by Duckworth & Kent Ltd.

Identity

Trade Name
Duckworth & Kent FDA UDI
Generic Name
Eyelid speculum, reusable FDA UDI
Device Name
Speculum EUDAMEDFDA UDI
Model / Reference
9-579 EUDAMEDFDA UDI
Description
Speculum FDA UDI

Identifiers

Catalog Number
9-579 FDA UDI
Primary DI / UDI-DI
05055313813804 EUDAMEDFDA UDI
Basic UDI-DI
B-05055313813804 EUDAMED
FDA Product Code
HNI FDA UDI
EMDN Code
L170102 OCULAR AND ENDOCULAR RETRACTORS, REUSABLE EUDAMED
GMDN Term
Eyelid speculum, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
Norway EUDAMED
Commercial Distribution
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

Speculum 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 10482a49-d89f-47bd-8ddc-98b301b7cb79 61 fields · synced Jun 19, 2026
  • FDA UDI de06fca3-954b-427a-a451-a3c0fd9f20e2 35 fields · synced May 30, 2026