- Organization name
- UDI-DI code
- Reference / catalog number
FR-MF-000001538URGO Sensitive-Stretch is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Laboratoires URGO HEALTHCARE. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jan 23, 2024
3664492LUHUS0015PEPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)03664492020457
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
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 Spain; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | — | Still on market |
| Belgium | — | Still on market |
| Czechia | — | Still on market |
| Estonia | — | Still on market |
| EL | — | Still on market |
| Italy | — | Still on market |
| Lithuania | — | Still on market |
| Latvia | — | Still on market |
| Poland | — | Still on market |
| Portugal | — | Still on market |
| Romania | — | Still on market |
| Slovenia | — | Still on market |
| Slovakia | — | Still on market |
| Türkiye | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03664492020457Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
3664492LUHUS0015PE3664492020457UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
M04010101NON-WOVEN ADHESIVE DRESSINGS, WITH ABSORBENT PADNo certificate specifically references this device's Basic UDI-DI.
3664492LUHUS0016PGOn the marketURGO RESISTANT3664492LUHUS0016PGOn the marketURGO SENSITIVE STRETCH3664492LUHUS0015PEOn the marketURGO Sensitive-Stretch3664492LUHUS0015PEOn the marketURGO SENSITIVE-STRETCH3664492LUHUS0015PEOn the marketURGO SENSITIVE-STRETCH3664492LUHUS0015PEOn the marketCertificate health across this manufacturer's portfolio.
10000452411-PA-NoMA-FRAIssuedNotified 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.
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