Organization name

Boston Scientific Corporation

SRN

US-MF-000004702

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

Sterling™

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.

08714729859956

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.

01915060000000000000361N3

Reference / catalog number

H74939032200610

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

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

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

Clinical sizes

• 150 MU10
• 2 MU50

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

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

• C010402020101PTA BALLOON DILATATION CATHETERS

• Class IIa medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

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