- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 13, 2026
697506955bandages9DPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →FARMA+LINE is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by JIANGSU JIELE MEDICAL DRESSING CO.,LTD. Placed on the EU market in Italy. 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 →06975069551173Basic 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 →697506955bandages9DCER3381AUDI 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)06975069551173
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.
M030101HYDROPHILIC GAUZE BANDAGESSterile
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 Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market |
CN-MF-000008773Certificate health across this manufacturer's portfolio.
HZ 2101147-1IssuedNotified 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.
View in glossary →B-06975069550756On the marketBCB-PARAFFIN GAUZE10cm x10cm(pack of 10)B-06975069550763On the marketBCB-PLAIN WHITE GAUZE SWABS 7.5cm x 7.5cm 8 ply( Pack of 5)697506955gauzespongesKCOn the marketBCB-PLAIN WHITE GAUZE SWABS 7.5cm x 7.5cm 8 ply( Pack of 5)697506955gauzespongesKCOn the marketCOMPRESSE DI GARZA 10x10cm697506955gauzesponges2VDOn the market