- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED data as of Aug 21, 2026
EUDAMED last updated this device on Nov 6, 2025
697570648113N4First aid bag Basic is an EU MDR-regulated medical device on the European market. It is classified as Class I. Manufactured by Bestreat Safety & First Aid Solution Co., Ltd.. Explore certificates, regulatory status and the official record on MD Atlas.
0697570648121499601F(01)06975706481214
European Medical Device Nomenclature — the EU product classification assigned to this device.
V9012NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USECN-PR-000032962The 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 DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
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.
UDI 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.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
No certificate specifically references this device's Basic UDI-DI.
697570648113N4On the marketExtra Mini Kit-IT697570648113N4On the marketExtra Mini Kit-PT697570648113N4On the marketFIRST AID BAG MINI BLUE697570648113N4On the marketFirst aid bag Plus697570648113N4On the marketFirst aid bag Plus Motorbike697570648113N4On 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.