Organization name

Baylis Medical Company Inc.

SRN

CA-MF-000024361

Manufacturer status

Active

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

• Refer to instruction manual/booklet
• Do not use past indicated date

Primary placement in Netherlands; available across 32 countries total.

Trade name

SureFlex™

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.

00685447018551

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-00685447018551

Reference / catalog number

TSK3003

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 III

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://www.ifu-bsci.com/

Clinical sizes

• 22 MU50

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

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

• C0502CARDIOVASCULAR INTRODUCER SHEATHS, VALVED

• Class III medical devices in EUDAMED

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