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EUDAMED last updated this device on Jun 5, 2026
69317478SP000011NTLithotomy Set, PRIMARY Plus is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Xuchang Zhengde Environstar Medical Products Co., Ltd.. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
CN-MF-000009427No 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)06931747858965
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.
CW009Sterile
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 Belgium; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Aug 30, 2026 | Dec 31, 2099 |
| Spain | Aug 30, 2026 | Dec 31, 2099 |
| France | Aug 30, 2026 | Dec 31, 2099 |
| Sweden | Aug 30, 2026 | Dec 31, 2099 |
| XI | Aug 30, 2026 | Dec 31, 2099 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06931747858965Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
69317478SP000011NT63890-00UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
T0202SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS)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.
69317478SP000011NTOn the marketLithotomy Set, PRIMARY69317478SP000011NTOn the marketLithotomy Set, PRIMARY69317478SP000011NTOn the marketLithotomy Set, PRIMARY Plus69317478SP000011NTOn the marketMAXILLOFACIAL SET69317478SP000022NYOn the marketMAXILLOFACIAL SET69317478SP000021NWOn the market