Prometheus FullStop Tourniquet - Hi Visibility PDF181
by Safeguard Medical Technologies Limited
Ref PDF181Model PDF180
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0506048357180S8 05060483570396 | Date28 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05060483570396 | Date4 May 2023 | StatusListed |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Prometheus FullStop Tourniquet - Hi Visibility
- Generic Name
- Limb tourniquet, manual, single-use
- Device Name
- Prometheus Fullstop Black
- Model / Ref / Catalog
- PDF181, PDF180
- Primary DI / UDI-DI
- 05060483570396
- Basic UDI-DI
- 0506048357180S8
- FDA Product Code
- GAX
- EMDN Code
- V9003 Tourniquets
- GMDN Term
- Limb tourniquet, manual, single-use
- Device Class
- Class I
- Regulation Number
- 878.5900
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Other devices from Safeguard Medical Technologies Limited
See all devices from Safeguard Medical Technologies Limited →
Properties
Other properties (19)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No