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

10-3540-K — Class I MDR by B.I.M.A. PLASTTEKNIK AB

MD Atlas
B.I.M.A. PLASTTEKNIK AB

EUDAMED last updated this device on May 25, 2026

10-3540-K

73400473(C)10-SERIESTR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: B.I.M.A. PLASTTEKNIK AB
UDI-DI code: 07340047333178
Reference / catalog number: 10-3540-K

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: B.I.M.A. PLASTTEKNIK AB
SRN: SE-MF-000001678
Manufacturer status: Active

Related devices

10-3535-PB-07340047300811On the market 10-3535-K7340047310-SERIESW4On the market 40-5247-K73400473(C)40-SERIESVWOn the market 40-5243-P73400473(C)40-SERIESVWOn the market 40-5555-P73400473(C)40-SERIESVWOn 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

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, 1990	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07340047333178
Basic UDI-DI: 73400473(C)10-SERIESTR
Reference / catalog number: 10-3540-K
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: Stadig, komfortabel och tryckfördelande rullstolsdyna, avsedd för personer som är beroende av rullstol för sina förflyttningar men kan variera sitt sittande. Medel till låg risk för trycksår. dynbasen är inkontinenssäker, överdraget är luftigt och bekvämt. Bima basic recond används när det är hög risk för inkontinens. Och då dynan ska kunna rekonditioneras till nyskick.
Additional information URL: https://bimasweden.se/produkter/bima-basic-recond/
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.

V080399MEDICAL CUSHIONS - 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