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

610120 — Class I MDR by Betterguards Technology…

MD Atlas
Betterguards Technology GmbH

EUDAMED last updated this device on Apr 28, 2026

610120

426235269TBGHH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Betterguards Technology GmbH
UDI-DI code: 04262352692760
Reference / catalog number: 610120

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: Betterguards Technology GmbH
SRN: DE-MF-000028712
Manufacturer status: Active

Related devices

710930426235269TBGHHOn the market 710930426235269TBGHHOn the market 710931426235269TBGHHOn the market 710931426235269TBGHHOn the market 710920426235269TBGHHOn 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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Anatomical conditions that prevent correct application; Lymph drainage disorders; Arterio-vascular disorders; Post-thrombotic conditions; Skin disease or skin irritation; Acute injuries or open wounds in ankle/foot area; Severe sensory disturbances; Polyneuropathy (e.g. diabetes mellitus); Post-traumatic/postoperative acute care. Caution: Before EVERY use, check mini-piston functionality. Do not use if defective.

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: 04262352692760
Basic UDI-DI: 426235269TBGHH
Reference / catalog number: 610120
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: No additional information URL provided by the manufacturer.
Clinical sizes: 20.5–23.5 MU10

EMDN nomenclature code(s)

Y061299LOWER EXTREMITY ORTHOSES - OTHER

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