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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

TP 3600 Duplex vacuum mattress set — Class I MDR by Mediseam Oy

MD Atlas
Mediseam Oy

EUDAMED last updated this device on Apr 4, 2025

TP 3600 Duplex vacuum mattress set

6430066193600W3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mediseam Oy
UDI-DI code: 06430066191086
Reference / catalog number: TP 3600

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Manufacturer information

Organization name: Mediseam Oy
SRN: FI-MF-000025545
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

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

Device identification

Trade name: TP 3600 Duplex vacuum mattress set
UDI-DI code: 06430066191086
Basic UDI-DI: 6430066193600W3
Reference / catalog number: TP 3600
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: TP 3600 Duplex vacuum mattress set The set includes TP360 vacuum mattress, a TP015 carrying bag and an AL450 vacuum mattress pump. TP 360 is a durable vacuum mattress designed for daily use. Strong and washing machine safe carry-on part that is manufactured of humidity protected fabric materials. Separately detachable vacuum part is inside the fabric covering. Detachable pillow for bracing the patient’s head. Six pairs of handles and four attachments with safety locks. Pistol valve. Dimensions 205 x 90 cm, weight 12,5 kgs.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 90 MU10
70 MU09
18 MU10
12.5 MU29

EMDN nomenclature code(s)

M03050299BANDAGES AND SPLINTS - 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

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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.