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EUDAMED last updated this device on May 26, 2026
69586949FYDSZSQ001G8PiC 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 Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0695869493501358071000090150(01)06958694935013
European Medical Device Nomenclature — the EU product classification assigned to this device.
A02010699INSULIN SYRINGES, SINGLE-USE - OTHER1 warning recorded — scroll inside the panel to see all entries.
(1)Before use, please check the integrity of the single package, single package leakage, damage and protective cover off, prohibit the use. (2)This product has been sterilized and used only for one-time use. It will be destroyed after use and the waste will be disposed of according to local government regulations. (3)Inject the human body immediately after aspirating the insulin solution. (4)This product is sterilized by EO for a period of validity of 5 years. When the product is in use, it is valid at the time of expiration of the package seal, and it is forbidden to use after expiration. (5)The injection site should be loose skin, such as upper arm, thigh, buttocks and abdomen. The injection site should alternate alternately. The same site cannot be injected twice in two weeks. Each injection site should be at least separated from the last injection site. 1cm or so. (6)Used by patients who is trained by doctors or professional doctors.
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary 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 →