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

10530 — Class I MDR by REBOTEC Rehabilitationsm…

MD Atlas
REBOTEC Rehabilitationsmittel GmbH

EUDAMED last updated this device on Mar 8, 2024

10530

4046678_GHMTSC-0001-130GV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: REBOTEC Rehabilitationsmittel GmbH
UDI-DI code: 04046678000146
Reference / catalog number: 10530

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: REBOTEC Rehabilitationsmittel GmbH
SRN: DE-MF-000009447
Manufacturer status: Active

Related devices

144164046678_GHGSxx-0003-125KMOn the market 144144046678_GHGSxx-0003-125KMOn the market 142104046678_GHGSxx-0003-125KMOn the market 144104046678_GHGSxx-0003-125KMOn the market 142164046678_GHGSxx-0003-125KMOn 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.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04046678000146
Basic UDI-DI: 4046678_GHMTSC-0001-130GV
Reference / catalog number: 10530
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: —
Additional information URL: https://www.rebotec.de/downloads
Clinical sizes: 130 MU29

EMDN nomenclature code(s)

Y12030601ELBOW CRUTCHES

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