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EUDAMED last updated this device on Apr 27, 2026
697462576QF03P5MEDPOREX ADHESIVE SURGICAL DRESSING 10x30CM(BOX OF 30) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Qidong Farjoy Medical Material Co., Ltd.. Placed on the EU market in Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
CN-MF-000012388(01)06974625762114
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 Ireland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| IrelandPrimary 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.
06974625762114Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
697462576QF03P5MD1154UDI 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.
M040499DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHERPrimary 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.
697462576QF03P5On the marketMEDISITE TRANSPARENT THIN FILM DRESSING 15X26CM (BOX OF 20)697462576QF03P5On the marketMEDPOREX ADHESIVE SURGICAL DRESSING 10x20CM(BOX OF 30)697462576QF03P5On the marketMEDPOREX ADHESIVE SURGICAL DRESSING 6x7CM(BOX OF 50)697462576QF03P5On the marketMEDPOREX ADHESIVE SURGICAL DRESSING 7x8CM(BOX OF 50)697462576QF03P5On the marketMEDPOREX ADHESIVE SURGICAL DRESSING 9x10CM(BOX OF 50)697462576QF03P5On the marketNo 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.