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EUDAMED last updated this device on Mar 4, 2026
69741004273004MDelantal EXTRA de Plástico Liso LDPE en BLOCK is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Uhealth Medical (Beijing) Products Co., Ltd.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
069741004212087300A1 packaging level registered — each level carries its own UDI-DI.
06974100421208× 100 unitsBase unit16974100421205× 5 units(01)06974100421208
European Medical Device Nomenclature — the EU product classification assigned to this device.
T0299PROTECTION DRAPES AND GARMENTS - OTHER1 warning recorded — scroll inside the panel to see all entries.
CN-MF-000043700The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Spain; available across 1 country total.
Placed on the market in Spain; per-country availability dates not published.
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 certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.69741004274004SOn the marketDelantal Desechable EXTRA de Polietileno LDPE Liso69741004274004SOn the marketDelantal Desechable EXTRA de Polietileno LDPE Liso69741004272004GOn the marketDiadema Desechable con Elásticos de Polipropileno697410042270046On the marketGorro Cirujano de Polipropileno Con Cintas697410042229048On the marketGorro de Polipropileno Detectable Plegado69741004221503POn the marketNo certificate specifically references this device's Basic UDI-DI.