- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Aug 31, 2026
8908004933SLSPF2M5CoreMed is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by St.Marys Rubbers Pvt. Ltd.. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
089044486062631LSPF-31752 packaging levels registered — each level carries its own UDI-DI.
08904448606263× 1 unitBase unit18904448606260× 50 units28904448606267× 10 units(01)08904448606263
European Medical Device Nomenclature — the EU product classification assigned to this device.
T01010102NON-POWDERED LATEX SURGICAL GLOVES4 warnings recorded — scroll inside the panel to see all entries.
This product contains natural rubber latex which may cause allergic reactions including anaphylactic responses in some individuals. In case of latex allergy , discontinue the use and consult a physician.
Risk of reuse : May cause infection, allergic reaction and poor barrier protection.
symbol
Sterile until package is opened or damaged
Primary placement in EL; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ELPrimary placement | Jun 1, 2026 | May 31, 2031 |
IN-MF-000008817The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
C556189IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →