- Role
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- Date of registration
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EUDAMED last updated this device on May 12, 2026
697178707SGNPUBSterix supremesoft PP, size 8.5 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Guilin HBM Health Protections, Inc.. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06933506092313697178707SGNPUB371GS185(01)06933506092313
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.
T01010101POWDERED LATEX SURGICAL GLOVES1 warning recorded — scroll inside the panel to see all entries.
CW009No certificate specifically references this device's Basic UDI-DI.
Primary placement in Türkiye; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | May 1, 2025 | Still on market |
CN-MF-000033439Certificate health across this manufacturer's portfolio.
M.2025.MDR.1086Issued