- Role
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EUDAMED last updated this device on May 20, 2026
08019020000000000000091KMPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →HEM-O-LOK APPLIER MEDIUM 11" CURVED REFURBISHED is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Teleflex Medical LLC.. Placed on the EU market in Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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 →14026704760807Basic 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 →08019020000000000000091KM544115RUDI 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 →(01)14026704760807
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
L020801MULTIPLE CLIPS APPLICATORS FOR OPEN SURGERY, REUSABLESterile
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 →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Ireland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| IrelandPrimary placement | Still on market |
US-MF-000023660No 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.08019020000000000000010JTOn the marketHEM-O-LOK APPLIER MEDIUM 11" 70 DEGREE ANGLE REFURBISHED08019020000000000000091KMOn the marketHEM-O-LOK APPLIER MEDIUM 11" CURVED08019020000000000000010JTOn the marketHEM-O-LOK APPLIER MEDIUM 8" CURVED08019020000000000000010JTOn the marketHEM-O-LOK APPLIER MEDIUM 8" CURVED REFURBISHED08019020000000000000091KMOn the marketHEM-O-LOK APPLIER MEDIUM LARGE 11" CURVED REFURBISHED08019020000000000000091KMOn the market