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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

0067002 — Class III MDD by Iberhospitex, S.A.

MD Atlas
Iberhospitex, S.A.

EUDAMED last updated this device on Jun 27, 2022

0067002

B-08428097931205

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Iberhospitex, S.A.
UDI-DI code: 08428097931205
Reference / catalog number: 0067002

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Manufacturer information

Organization name: Iberhospitex, S.A.
SRN: ES-MF-000000160
Manufacturer status: Active

Related devices

0068001B-08428097953108On the market 0067003B-08428097931304On the market 0067001B-08428097931106On the market 0067102B-08428097931502On the market 0067103B-08428097931601On the market

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW020
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Jun 29, 2020	Still on market
Croatia	Sep 20, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08428097931205
Basic UDI-DI: B-08428097931205
Reference / catalog number: 0067002
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC 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: 10 MU50
1.25 MU50

EMDN nomenclature code(s)

C010401020101PTCA BALLOON DILATION CATHETERS

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

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.