- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 18, 2026
697282318STDRAPESQVBARAMEDA Under buttock drape EL75100 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Excellent Medical Technology Group Co., Ltd.. Placed on the EU market in Lithuania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
36972823187846GS1 ChinaCN-MF-000022462No certificate specifically references this device's Basic UDI-DI.
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.(01)36972823187846
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
CW010Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Lithuania; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| LithuaniaPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
T020102SPECIALISTIC SURGERY DRAPESPrimary 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 →697282318EXTREKITRQOn the marketBARAMEDA Extremity Set ART-5C697282318EXTREKITRQOn the marketBARAMEDA TUR set ETURS-3697282318UROPACKBHOn the marketBARAMEDA Universal set EUNIVS-1C+G697282318UNIKITWXOn the marketCures disposable set L (latex) 0026077EM697282318CURESKITS8NOn the marketCures disposable set L (nitrile) 0026066EM697282318CURESKITS8NOn the market