- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 23, 2026
69506261FQ01SNNNSBDP0007TSterile basic dressing pack is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Shaoxing Fuqing Health Products Co., Ltd.. Placed on the EU market in Slovenia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06950626180676BDP205ECN-MF-000007338(01)06950626180676
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 Slovenia; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| SloveniaPrimary placement | Jan 1, 2020 | Jan 28, 2031 |
| Croatia | Jan 1, 2020 | Jan 28, 2031 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
M9099GENERAL AND SPECIALIST MEDICAL DEVICES – OTHER (SUTURE PATCHES SEE H900102)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.
69506261FQ01NNNNSNS000068On the marketNon-woven swabs69506261FQ01NNNNSNS000068On the marketReliance Maternity Pack - Sterile PackB-06950626173784On the marketSterile Gauze Swab69506261FQ01SNNNSGS000088On the marketTrokutna marama69506261FQ01NNNNSBB0000TEOn the marketNS100N69506261FQ01NNNNSNS000068On 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.