- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 11, 2026
20221SYRSFT261TXEXEL Disposable Syringe with SecureTouch Safety Needle, 3mL Luer Lock Tip W/ 23G X 5/8” is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Exelint International, Co.. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
US-MF-000037396No 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.(01)00020221271188
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
5 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW001CW032CW007Sterile
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 Austria; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary 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.
00020221271188Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
20221SYRSFT261TX27118UDI 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.
A02010205INFUSION AND IRRIGATION SYRINGES WITH SAFETY SYSTEM, SINGLE-USEPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →20221SYRSFT261TXOn the marketEXEL Disposable Syringe with SecureTouch Safety Needle, 3mL Luer Lock Tip W/ 23G X 1-1/2”20221SYRSFT261TXOn the marketEXEL Disposable Syringe with SecureTouch Safety Needle, 3mL Luer Lock Tip W/ 23G X 1”20221SYRSFT261TXOn the marketEXEL Disposable Syringe with SecureTouch Safety Needle, 3mL Luer Lock Tip W/ 25G X 1-1/2”20221SYRSFT261TXOn the marketEXEL Disposable Syringe with SecureTouch Safety Needle, 3mL Luer Lock Tip W/ 25G X 1”20221SYRSFT261TXOn the marketEXEL Disposable Syringe with SecureTouch Safety Needle, 3mL Luer Lock Tip W/ 25G X 5/8”20221SYRSFT261TXOn the marketNo certificate specifically references this device's Basic UDI-DI.