Elabo

Organization name

YURIM MEDICAL Co., Ltd.

SRN

KR-MF-000009011

Manufacturer status

Active

9 warnings recorded — scroll inside the panel to see all entries.

• Caution
• Caution, sharp edges
• Consult instructions for use
• Avoid contact with non-sterile water
• Do not re-use
• Do not resterilize
• Do not use if package is damaged
• Do not use past indicated date
• Do not sterilise

Primary placement in Poland; available across 13 countries total.

Trade name

Elabo

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

08809684739488

Basic UDI-DI

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.

B-08809684739488

Reference / catalog number

YC-22-50

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

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.

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

C-Type / 22G 50mm

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 22G
• 50mm

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• A0101010102HYPODERMIC SYRINGE NEEDLES, W/O SAFETY SYSTEMS

• Class IIa medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.

Certificate health across this manufacturer's portfolio.