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FOI – 2022-000077 Marketing And Communications team
Information request and response for FOI Reference: FOI – 2022-000077
MHRA Medical Device Safety Information – MDSI2309
MDSI2309 - BioIntegral Surgical Inc. No-React® cardiovascular bioprosthesis implantables: discontinuation of CE marking and manufacture
How we implement new frameworks at the distribution centre
Find out how the National Distribution Centre transfers to new products once frameworks are awarded and what you need to do.
How we implement new frameworks at the distribution centre
Find out how the National Distribution Centre transfers to new products once frameworks are awarded and what you need to do.
Device Safety Information – DSI/2025/001
DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate
National programme delivery
Learn how Portfolio Services can design and deliver a programme to suit your needs.
MHRA Device Safety Information – MDSI2306
MDSI2306 - NuVasive Specialized Orthopedics (NSO) PRECICE Titanium Systems: UK Suspension Lifted
Apply for tender opportunities
Use PCS-Tender to apply for a national healthcare tender. It's a secure eTendering system funded by the Scottish government.
Safety Information Message – SIM2501(U)
SIM2501(U) - Product Safety Report: MK Electric MK Essentials Electrical Three Pin Sockets with Switches: risk of burns
MHRA Medical Device Safety Information – MDSI2311U
MDSI2311U - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel: potential risk of infection - UPDATE