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EUDAMED last updated this device on Apr 22, 2026
693811933359JFSAN25 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by Henan Tuoren Medical Device Co., Ltd. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06941617117818693811933359JFSAN25(01)06941617117818
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
A01030101SPINAL ANAESTHESIA NEEDLES AND KITS7 warnings recorded — scroll inside the panel to see all entries.
CW011CW010CW009CW001CW007CW032CW136Primary placement in Italy; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market | |
| Germany | Still on market | |
| Spain | Still on market | |
| France | Still on market |
CN-MF-000013924Certificate health across this manufacturer's portfolio.
28620228213Issued28620228214Issued28620228214