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Susol® Digital Tourniquet

EUDAMEDFDA UDI

Class I (EU MDR)

Ref S-TQS

by Bailey Instruments Ltd.

Identity

Trade Name
Susol® Digital Tourniquets Small Orange FDA UDI
Generic Name
Digit tourniquet, manual FDA UDI
Device Name
Susol® Digital Tourniquet EUDAMED
Model / Reference
S-TQS EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05060418833541 EUDAMED
05060418834869 FDA UDI
Basic UDI-DI
506041883SSENT3746823 EUDAMED
Unit of Use DI
05060418834869 EUDAMED
FDA Product Code
GAX FDA UDI
EMDN Code
V901699 SPECIALIST SURGICAL INSTRUMENTS AND KITS NOT INCLUDED IN OTHER CLASSES, SINGLE-USE - OTHER EUDAMED
GMDN Term
Digit tourniquet, manual FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.5900 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® Digital Tourniquet 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 0c242a7e-3d60-4249-b661-c99363a70e4e 61 fields · synced Jun 20, 2026
  • FDA UDI 1fbb733a-fe61-4d96-bc41-b54a3c0bfec8 32 fields · synced May 24, 2026