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EUDAMED last updated this device on Apr 10, 2026
69586976HWZSZ0017BRAYS NEEDLE 22GX2"(0.7 X 50mm) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Anhui Hongyu Wuzhou Medical Manufacturer CO.,Ltd.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06958697613383HN22G50CN-MF-000029789(01)06958697613383
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
4 warnings recorded — scroll inside the panel to see all entries.
CW275CW029CW009CW007Sterile
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 Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
A0101010102HYPODERMIC SYRINGE NEEDLES, W/O SAFETY SYSTEMSPrimary 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.
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.69586976HWZSQ0015COn the marketPOLnet-MED SYRINGE, 3 PARTS,2ML/3ML69586976HWZSQ0015COn the marketPOLnet-MED SYRINGE, 3 PARTS,5ML/6ML69586976HWZSQ0015COn the marketRAYS SAFETY HYPODERMIC NEEDLE 22G x 1" (0.7 x 25mm)69586976HWAQZSZ002GCOn the marketRAYS SAFETY HYPODERMIC NEEDLE 18G x 1 1/2" (1.2 x 38mm)69586976HWAQZSZ002GCOn the marketRAYS SAFETY HYPODERMIC NEEDLE 19G x 1 1/2" (1.1 x 38mm)69586976HWAQZSZ002GCOn the market