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Susol

EUDAMED

Class I (EU MDR)

Ref BSDP-01A

by Bailey Instruments Ltd.

Identity

Trade Name
Susol EUDAMED
Device Name
Susol® Podiatry Set EUDAMED
Model / Reference
BSDP-01A EUDAMED

Identifiers

Primary DI / UDI-DI
05060418834876 EUDAMED
Basic UDI-DI
506041883SSGEN56303TD EUDAMED
EMDN Code
V901699 SPECIALIST SURGICAL INSTRUMENTS AND KITS NOT INCLUDED IN OTHER CLASSES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Category: General internal orthopaedic fixation system implantation kit

Susol by Bailey Instruments Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
GB-MF-000013119
Authorised Representative
MD REPS Ltd XI-AR-000040375

Sources (1)

  • EUDAMED a2192ed5-6ce2-4bc1-baa1-f57728b7fd7b 61 fields · synced May 23, 2026