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EUDAMED last updated this device on May 22, 2026
69586949DJMSYZ001FVMetze is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Jiangsu Jichun Medical Devices CO.,Ltd. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
36958694904249JM2770MP(01)36958694904249
European Medical Device Nomenclature — the EU product classification assigned to this device.
A01010202BUTTERFLY NEEDLES, W/O SAFETY SYSTEMS1 warning recorded — scroll inside the panel to see all entries.
1) This product is sterilized by Ethylene oxide; 2) Before use, please check the integrity of the single packing, if any leakage, damage and the drop off of the protective cap, please do not use; 3) This product is sterilized and can be used only for once, please destroy after use; 4) The operation shall be implemented and warded by professional nursing staff; 5) This product is not fit for infusion fat-soluble liquid and medicine, such as fat milk; 6) It is forbidden to infusion the medicine incompatible to PVC; 7) According to the foreign research data, the clinical medical staff shall pay attention to that the PVC tubing will interact with the infused medicine, to cause the possible change of the medicine effect; 8) The valid period of the product is 5 years after EO sterilization, during use, please read clearly the expiry date at the sealing of the single packing, please do not use after the valid date.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
CN-MF-000019298The 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.
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 certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
DZ 2049691-1SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →