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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

E1001707 — Class IIb MDR by Honeywell Healthcare…

MD Atlas
Honeywell Healthcare Solutions GmbH

EUDAMED last updated this device on Jun 15, 2023

E1001707

4036616SpO2MonEQ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Honeywell Healthcare Solutions GmbH
UDI-DI code: 04036616009034
Reference / catalog number: E1001707

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Manufacturer information

Organization name: Honeywell Healthcare Solutions GmbH
SRN: DE-MF-000004924
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Apr 1, 2007	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04036616009034
Basic UDI-DI: 4036616SpO2MonEQ
Reference / catalog number: E1001707
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: OxiPen ohne Sensor
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z1203020408PULSE OXIMETERS

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

Related devices

01-00-00134036616OOMCKOn 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.