- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jul 7, 2026
B-00870053000445GuardaCare PRO 2"x2", 8ply is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by Tricol Biomedical Inc. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
008700530004451012 (IT)(01)00870053000445
European Medical Device Nomenclature — the EU product classification assigned to this device.
M040501POLYSACCHARIDE HAEMOSTATIC DRESSINGSM0202010101NON-WOVEN FOLDED GAUZES, WITHOUT X-RAY DETECTABLE THREAD, STERILE12 warnings recorded — scroll inside the panel to see all entries.
OTHER
For external use only; Do not implant
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Feb 23, 2006 | Still on market |
US-MF-000002003252.690OTHER
OTHER
OTHER
OTHER
OTHER
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.
B-00870053000384On the marketChitoGauze XR PRO, SafeguardB-00870053000018On the marketGuardaCare PRO 2"x2", 8plyB-00870053001350On the marketGuardaCare PRO 2"x2", 8plyB-00870053000513On the marketGuardaCare PRO 4"x4", 8plyB-00870053000520On the marketGuardaCare PRO 4"x4", 8plyB-00870053000452On the marketNo 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.