- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 20, 2026
08019020000000000000092KPHEM-O-LOK REMOVER LARGE/EXTRA LARGE 11" 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.
14026704760821544124RUS-MF-000023660(01)14026704760821
The 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.
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 Ireland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| IrelandPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
L21CLIP REMOVAL SURGICAL FORCEPS, REUSABLEPrimary 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 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.No certificate specifically references this device's Basic UDI-DI.
08019020000000000000008K8On the marketHEM-O-LOK OPEN UNIVERSAL REMOVER 8" REFURBISHED08019020000000000000092KPOn the marketHEM-O-LOK REMOVER LARGE/EXTRA LARGE 11"08019020000000000000008K8On the marketHEM-O-LOK REMOVER, EXTRA LARGE/LARGE ENDOSCOPIC08019020000000000000007K6On the marketHEM-O-LOK TAP 10 MILIMETER ENDOSCOPIC REMOVER08019020000000000000009KAOn the marketHEM-O-LOK TAP 5 MILIMETER ENDOSCOPIC REMOVER08019020000000000000009KAOn the market