- Organization name
- UDI-DI code
- Reference / catalog number
IT-MF-000010693SOFFISOF DERMO SAGOMATO AIR DRY SUPER 8 GOCCE 2X30 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Società Italiana Lavorazione Cellulosa SpA. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Aug 24, 2026
8007300FAM0000006YYPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08007300011486
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 Italy; available across 12 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jul 1, 2026 | Still on market |
| Belgium | Jul 1, 2026 | Still on market |
| Bulgaria | Jul 1, 2026 | Still on market |
| Czechia | Jul 1, 2026 | Still on market |
| Germany | Jul 1, 2026 | Still on market |
| Estonia | Jul 1, 2026 | Still on market |
| EL | Jul 1, 2026 | Still on market |
| France | Jul 1, 2026 | Still on market |
| Croatia | Jul 1, 2026 | Still on market |
| Portugal | Jul 1, 2026 | Still on market |
| Slovenia | Jul 1, 2026 | Still on market |
| XI | Jul 1, 2026 | 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.
08007300011486Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
8007300FAM0000006YY01148UDI 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.
T04010102SHAPED INCONTINENCE NAPPIES8007300FAM0000006YYOn the marketSOFFISOF DERMO SAGOMATO AIR DRY MAXI 9 GOCCE 2X308007300FAM0000006YYOn the marketSOFFISOF DERMO SAGOMATO AIR DRY PLUS 6 GOCCE 4X308007300FAM0000006YYOn the marketSOFFISOF LADY AIR DRY EXTRA 18X10 PCS8007300FAM0000003YSOn the marketSOFFISOF LADY AIR DRY NORMAL 20X12 PCS8007300FAM0000003YSOn the marketSOFFISOF LADY AIR DRY SUPER 8X15 PCS8007300FAM0000003YSOn the marketNo certificate specifically references this device's Basic UDI-DI.
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.