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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

Digitemp — Class I MDR by EQUA OÜ

MD Atlas
EQUA OÜ

EUDAMED last updated this device on Dec 10, 2021

Digitemp

4745010252H711033CU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EQUA OÜ
UDI-DI code: 04745010252051
Reference / catalog number: H711033

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Manufacturer information

Organization name: EQUA OÜ
SRN: EE-MF-000000705
Manufacturer status: Active

Related devices

H7110314745010252H711031CQOn the market H711033-84745010252H711033-8GAOn the market H711032-84745010252H711032-8G5On the market H7110324745010252H711032CSOn the market H7110344745010252H711034CWOn 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.

Market distribution

Primary placement in Estonia; available across 1 country total.

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

Device identification

Trade name: Digitemp
UDI-DI code: 04745010252051
Basic UDI-DI: 4745010252H711033CU
Reference / catalog number: H711033
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.

EMDN nomenclature code(s)

T030199COVERS, INSTRUMENTS AND 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification