Organization name

Hill-Rom, Inc.

SRN

US-MF-000007306

Manufacturer status

Active

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

• CW016

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW011

  EUDAMED did not publish a description for this code.

Primary placement in France; available across 31 countries total.

Trade name

Progressa

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.

00887761000100

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.

0887761GMN000043U6

Reference / catalog number

P7500

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

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

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

• V08060199ELECTRIC MEDICAL BEDS - OTHER
• V08060105ELECTRIC MEDICAL BEDS WITH WEIGHING SYSTEM
• V08060102INTENSIVE CARE OR RESUSCITATION ELECTRIC MEDICAL BEDS

• Class IIa medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.