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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

Freedom 200 — Class I MDR by IHBO B.V.

MD Atlas
IHBO B.V.

EUDAMED last updated this device on Mar 31, 2022

Freedom 200

08417361F4-CMS-NOGAS-I-CK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: IHBO B.V.
UDI-DI code: 10841736121082
Reference / catalog number: Freedom 200

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Manufacturer information

Organization name: IHBO B.V.
SRN: NL-MF-000000062
Manufacturer status: Active

Related devices

Freedom 10008417361F4-CMS-NOGAS-I-CKOn the market Freedom 100-MGS08417361F4-CMS-GAS-IIa-35On the market Freedom 200-MGS08417361F4-CMS-GAS-IIa-35On the market Freedom 30008417361F4-CMS-NOGAS-I-CKOn the market Freedom 300-MGS08417361F4-CMS-GAS-IIa-35On 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.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Feb 18, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 10841736121082
Basic UDI-DI: 08417361F4-CMS-NOGAS-I-CK
Reference / catalog number: Freedom 200
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.

V0899MEDICAL SUPPORT EQUIPMENT - 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

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