Identity
- Trade Name
- Susol® Digital Tourniquets Medium Green (Pack of 50) FDA UDI
- Generic Name
- Digit tourniquet, manual FDA UDI
- Device Name
- Susol® Digital Tourniquet EUDAMED
- Model / Reference
- S-TQM EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 05060418833534 EUDAMED05060418834852 FDA UDI
- Basic UDI-DI
- 506041883SSENT3746823 EUDAMED
- Unit of Use DI
- 05060418834852 EUDAMED
- FDA Product Code
- GAX FDA UDI
- EMDN Code
- V901603 SUPERFICIAL TREATMENTS INSTRUMENTS AND KITS, SINGLE-USE 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
Susol® Digital Tourniquet by Bailey Instruments Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 506041883SSENT3746823 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Bailey Instruments Ltd.
- EUDAMED SRN
- GB-MF-000013119
- Authorised Representative
- MD REPS Ltd XI-AR-000040375
Sources (2)
- EUDAMED 1e6432ec-cf3b-47af-8b27-993e0d51fcd3 61 fields · synced May 31, 2026
- FDA UDI 932c9600-60d0-4d62-9193-4ba2b8be4f50 32 fields · synced May 30, 2026