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

DÄCK 2.80/2.50-4 FYLLD PRIMO — Class I MDR by Haco Tellus AB

MD Atlas
Haco Tellus AB

EUDAMED last updated this device on May 26, 2026

DÄCK 2.80/2.50-4 FYLLD PRIMO

7330530SF001LY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Haco Tellus AB
UDI-DI code: 07330530002001
Reference / catalog number: 4500035

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: Haco Tellus AB
SRN: SE-MF-000053610
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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.

Country	On market since	Until
SwedenPrimary placement	Jan 1, 2024	Still on market

Device identification

Trade name: DÄCK 2.80/2.50-4 FYLLD PRIMO
UDI-DI code: 07330530002001
Basic UDI-DI: 7330530SF001LY
Reference / catalog number: 4500035
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: No clinical sizes registered for this device.

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.

Y122499WHEELCHAIRS ACCESSORIES - 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

Become a partner of MD Atlas

Related devices

A2M-NEK 100X32 OA 10 MM BÄRF 80 KG7330530MF001JWOn the market A2M-NEK 125X32 OA 10 MM BÄRF 100 KG7330530MF001JWOn the market A2M-NEK 125X32 OA 10 MM BÄRF 100 KG7330530MF001JWOn the market A2M-NEK 150X32 OA 12 MM BÄRF 105 KG7330530MF001JWOn the market A2M-NEK 150X32 OA 12 MM PLASTBROMS7330530MF001JWOn 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.