Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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

Customized Kneesupport Neoprene L — Class I MDR

MD Atlas
Customized innovations i Sverige AB

EUDAMED last updated this device on Jun 18, 2025

Customized Kneesupport Neoprene L

735012084Knee01MQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Customized innovations i Sverige AB
UDI-DI code: 07350120844965
Reference / catalog number: CCS8020L

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?

View device family (Basic UDI)

Manufacturer information

Organization name: Customized innovations i Sverige AB
SRN: SE-MF-000047918
Manufacturer status: Active

Related devices

Customized Ankle Support L735012084Ankle0147On the market Customized Ankle Support M735012084Ankle0147On the market Customized Ankle Support S735012084Ankle0147On the market Customized Ankle Support XL735012084Ankle0147On the market Customized Back Support L735012084Back01E4On 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.

CW010
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Sweden; available across 1 country total.

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

Device identification

Trade name: Customized Kneesupport Neoprene L
UDI-DI code: 07350120844965
Basic UDI-DI: 735012084Knee01MQ
Reference / catalog number: CCS8020L
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: A soft, adjustable neoprene knee brace featuring metal reinforcement and a silicone ring for compression and stabilization. Equipped with a Velcro strap to optimize fit and support.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: L

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

Y061209KNEE ORTHOSES

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

Become a partner of MD Atlas