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

91253 — Class I MDR by HOYER GmbH

MD Atlas
HOYER GmbH

EUDAMED last updated this device on May 11, 2026

91253

42607410291XXXTuch75

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HOYER GmbH
UDI-DI code: 04260741024031
Reference / catalog number: 91253

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: HOYER GmbH
SRN: DE-MF-000007883
Manufacturer status: Active

Related devices

71765426074102schienensystemHQOn the market 9182042607410291XXXTuch75On the market 9181942607410291XXXTuch75On the market 9182142607410291XXXTuch75On the market 71751426074102schienensystemHQOn the market

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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260741024031
Basic UDI-DI: 42607410291XXXTuch75
Reference / catalog number: 91253
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: 36-Fell 1k * *Ein Stück* AD-Fellüberzug für 36-Po Gurt kurz 114cm , Normalbreite Himi.- Nr.: 22.40.04.0001
Additional information URL: http://hoyer-lifter.com/36-po-gurtpaar.html
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0805038002NON-RIGID SUPPORTS FOR LIFTS (HARNESSES)

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