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EUDAMED last updated this device on Mar 26, 2026
69553561SNSLA29SECURISEE UNITE DE PRELEVEMENT 19CM 21G is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Gemtier Medical (Shanghai) Inc.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
16955356121958105420(01)16955356121958
European Medical Device Nomenclature — the EU product classification assigned to this device.
A010199NEEDLES FOR INFUSION AND COLLECTION - OTHERCN-MF-000003835The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Jan 28, 2019 | Still on market |
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.
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.69553561SNSLH2POn the marketSafety Blood Collection Set with Tube Holder, 30cm tubing, 23G needle69553561SNSLH2POn the marketSafety Blood Collection Set with Tube Holder, 30cm tubing, 25G needle69553561SNSLH2POn the marketSECURISEE UNITE DE PRELEVEMENT 19CM 23G69553561SNSLA29On the marketSterile Syringe with Safety Needle for Single Use, 1ml syringe, 25Gx25mm needle69553561SYDEN2GOn the marketTube Holder69553561SNSLH2POn the market