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Prometheus FullStop Tourniquet - Black
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref PDF181Model PDF180
Identity
- Trade Name
- Prometheus FullStop Tourniquet - Black FDA UDIPrometheus FullStop Tourniquet - Hi Visibility FDA UDI
- Generic Name
- Limb tourniquet, manual, single-use FDA UDI
- Device Name
- PROMETHEUS FULLSTOP BLACK EUDAMEDThe Prometheus FullStop® tourniquet is a lightweight, durable tourniquet that has been shown to successfully occlude arterial blood flow. FDA UDI
- Model / Reference
- PDF180 EUDAMEDFDA UDIPDF181 EUDAMEDFDA UDI
- Description
- The Prometheus FullStop® tourniquet is a lightweight, durable tourniquet that has been shown to successfully occlude arterial blood flow. FDA UDI
Identifiers
- Catalog Number
- PDF180 FDA UDIPDF181 FDA UDI
- Primary DI / UDI-DI
- 05060483570389 EUDAMEDFDA UDI05060483570396 EUDAMEDFDA UDI
- Basic UDI-DI
- 0506048357180S8 EUDAMED
- FDA Product Code
- GAX FDA UDI
- EMDN Code
- V9003 TOURNIQUETS EUDAMED
- GMDN Term
- Limb tourniquet, manual, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.5900 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Category: Limb tourniquet, manual, single-use
Prometheus FullStop Tourniquet - Black by Safeguard Medical Technologies Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Safeguard Medical Technologies Limited
Sources (4)
- FDA UDI 27ec681b-6d0f-4b06-91ee-4bbf67f7eb0b 35 fields · synced Sep 18, 2026
- FDA UDI fdfb3c17-c817-4b00-a828-2becffd13616 35 fields · synced May 30, 2026
- EUDAMED 41ef98f9-51eb-42d0-aba7-7cf061bb4b4d 61 fields · synced Jul 9, 2026
- EUDAMED 1d0c008a-c2b9-48d5-9999-35367b501dbd 61 fields · synced Sep 18, 2026