Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

IMR-HLL-nn — Class I MDR by Ergotrics

MD Atlas
Ergotrics

EUDAMED last updated this device on Aug 21, 2025

IMR-HLL-nn

5430001965IMRYQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ergotrics
UDI-DI code: 05430001965452
Reference / catalog number: IMR-HLL-nn

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Ergotrics
SRN: BE-MF-000024176
Manufacturer status: Active

Related devices

COV-PAU-nn5430001965COVY8On the market HMB-AAA-nn5430001965HMBXKOn the market HMB-DAA-nn5430001965HMBXKOn the market IBO-EOL-nn5430001965IBOXHOn the market IMC-HLD-nn5430001965IMCXSOn the market

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement		Still on market

Device identification

Trade name: IMR-HLL-nn
UDI-DI code: 05430001965452
Basic UDI-DI: 5430001965IMRYQ
Reference / catalog number: IMR-HLL-nn
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Morpheroll
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12011280PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No 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.