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EUDAMED last updated this device on Jul 3, 2026
694878812001PVCompresse de Gaze 10x10cm 32plis 17 fils avec X-ray detectable is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Hubei Qianjiang Kingphar Medical Material Co., Ltd. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
CN-MF-000009051(01)06948788181006
The 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.
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 France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06948788181006Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
694878812001PV1116S2X-FEUDI 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.
M0201050201COTTON GAUZE PADS, WITH X-RAY DETECTABLE THREAD, STERILEPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →694878812014Q6On the marketabsorbent pads694878812014Q6On the marketCompressa di garza sterile694878811*005E4On the marketCompresse de Gaze 10x10cm 32plis 17 fils avec X-ray detectable694878812001PVOn the marketCompresse de Gaze 10x20cm 24plis 17 fils avec X-ray detectable694878812001PVOn the marketCompresse de Gaze de coton 45x45cm 4 plis 17 fils694878812006Q7On the marketNo certificate specifically references this device's Basic UDI-DI.
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.