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Susol

EUDAMEDFDA UDI

Class I (EU MDR)

Ref SS09-0625Model SS30-2601

by Bailey Instruments Ltd.

Identity

Trade Name
Susol EUDAMED
Susol® Forceps Artery Halstead Mosquito Straight 12.5cm FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, single-use FDA UDI
Device Name
Susol® Forceps Magill Intubation Adult 24cm EUDAMED
Model / Reference
SS30-2601 EUDAMED
SS09-0625 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05060418832803 EUDAMED
05060418834128 FDA UDI
Basic UDI-DI
506041883REGEN11791FA EUDAMED
Unit of Use DI
05060418834128 EUDAMED
FDA Product Code
GEN FDA UDI
EMDN Code
V901699 SPECIALIST SURGICAL INSTRUMENTS AND KITS NOT INCLUDED IN OTHER CLASSES, SINGLE-USE - OTHER EUDAMED
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General internal orthopaedic fixation system implantation kit

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

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 63f3a77f-c29b-48f7-83d2-8ae85def65c9 61 fields · synced Jun 8, 2026
  • FDA UDI 3df9caaf-49fb-4ecb-9903-11d74b014e0a 32 fields · synced May 29, 2026