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EUDAMED last updated this device on Jun 4, 2026
858601504BCN108LTECROM 0,80x25mm (21Gx1”) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by CHIRANA T.Injecta, a.s.. Placed on the EU market in Denmark. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
07503058219620TCBCN21100(01)07503058219620
European Medical Device Nomenclature — the EU product classification assigned to this device.
A01010502NEEDLES FOR COLLECTION UNDER VACCUM, W/O SAFETY SYSTEMS3 warnings recorded — scroll inside the panel to see all entries.
CW009CW001CW007Primary placement in Denmark; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| DenmarkPrimary placement | — | Still on market |
SK-MF-0000037022022-MDR/QS-025/CThe 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 →858601504BCN108LOn the marketTECROM 0,70x25mm (22Gx1”)858601504BCN108LOn the marketTECROM 0,70x38mm (22Gx1 1/2”)858601504BCN108LOn the marketTECROM 0,80x38mm (21Gx1 1/2”)858601504BCN108LOn the marketTECROM 0,90x25mm (20Gx1”)858601504BCN108LOn the marketTECROM 0,90x38mm (20Gx1 1/2”)858601504BCN108LOn the marketCertificate health across this manufacturer's portfolio.
2022-MDR/QS-024/BSupplementedNotified 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.
2022-MDR/QS-025/CSupplementedNotified 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.
2022-MDR/QS-026/DSupplementedNotified 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.
2022-MDR/QS-027/ASupplementedNotified 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.
2024-MDR/QS-071IssuedNotified 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.
2022-MDR/QS-025IssuedNotified 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 →