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Organization name
UDI-DI code
Reference / catalog number

Arthroscopy drape — Class I MDR by Oasipor - Medical, S.A.

MD Atlas
Oasipor - Medical, S.A.

EUDAMED last updated this device on May 21, 2026

Arthroscopy drape

560032008CC21XPC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Oasipor - Medical, S.A.
UDI-DI code: 05600320080482
Reference / catalog number: 214122

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View device family (Basic UDI)

Manufacturer information

Organization name: Oasipor - Medical, S.A.
SRN: PT-MF-000002957
Manufacturer status: Active

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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.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement		Still on market

Device identification

Trade name: Arthroscopy drape
UDI-DI code: 05600320080482
Basic UDI-DI: 560032008CC21XPC
Reference / catalog number: 214122
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: Arthroscopy drap withfluid collecton pouch - 320 x 220 cm - Arjo wrap
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.

T020102SPECIALISTIC SURGERY DRAPES

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

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