EUDAMED last updated this device on May 19, 2026

Temperature probe

69449040AB010000513F

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
UDI-DI code: 06944904099835
Reference / catalog number: MR403B(040-003736-00)

Temperature probe is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on May 19, 2026

Temperature probe

69449040AB010000513F

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
UDI-DI code: 06944904099835
Reference / catalog number: MR403B(040-003736-00)

View device family (Basic UDI)

Device identification

Trade name: Temperature probe
UDI-DI code: 06944904099835
Basic UDI-DI: 69449040AB010000513F
Reference / catalog number: MR403B(040-003736-00)
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

UDI-DI DataMatrix

Encoded

(01)06944904099835

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V03010201TEMPERATURE MONITORING CUTANEOUS PROBES

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
Follow the instructions for use and adhere to all warnings and cautions.

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

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in Germany; available across 32 countries total.

Country	On market since	Until
GermanyPrimary placement	Aug 5, 2015	Aug 5, 2065
Austria	Aug 5, 2015	Aug 5, 2065
Belgium	Aug 5, 2015	Aug 5, 2065
Bulgaria	Aug 5, 2015	Aug 5, 2065
Cyprus	Aug 5, 2015	Aug 5, 2065
Czechia	Aug 5, 2015	Aug 5, 2065
Denmark	Aug 5, 2015	Aug 5, 2065
Estonia	Aug 5, 2015	Aug 5, 2065
EL	Aug 5, 2015	Aug 5, 2065
Spain	Aug 5, 2015	Aug 5, 2065
Finland	Aug 5, 2015	Aug 5, 2065
France	Aug 5, 2015	Aug 5, 2065
Croatia	Aug 5, 2015	Aug 5, 2065
Hungary	Aug 5, 2015	Aug 5, 2065
Ireland	Aug 5, 2015	Aug 5, 2065
Iceland	Aug 5, 2015	Aug 5, 2065
Italy	Aug 5, 2015	Aug 5, 2065
Liechtenstein	Aug 5, 2015	Aug 5, 2065
Lithuania	Aug 5, 2015	Aug 5, 2065
Luxembourg	Aug 5, 2015	Aug 5, 2065
Latvia	Aug 5, 2015	Aug 5, 2065
Malta	Aug 5, 2015	Aug 5, 2065
Netherlands	Aug 5, 2015	Aug 5, 2065
Norway	Aug 5, 2015	Aug 5, 2065
Poland	Aug 5, 2015	Aug 5, 2065
Portugal	Aug 5, 2015	Aug 5, 2065
Romania	Aug 5, 2015	Aug 5, 2065
Sweden	Aug 5, 2015	Aug 5, 2065
Slovenia	Aug 5, 2015	Aug 5, 2065
Slovakia	Aug 5, 2015	Aug 5, 2065
Türkiye	Aug 5, 2015	Aug 5, 2065
XI	Aug 5, 2015	Aug 5, 2065

Device identification

Trade name: Temperature probe
UDI-DI code: 06944904099835
Basic UDI-DI: 69449040AB010000513F
Reference / catalog number: MR403B(040-003736-00)
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.

Manufacturer information

Organization name: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
SRN: CN-MF-000014156
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06944904099835

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V03010201TEMPERATURE MONITORING CUTANEOUS PROBES

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
Follow the instructions for use and adhere to all warnings and cautions.

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

Certificates

Certificate health across this manufacturer's portfolio.

CN26/00002236Issued
Quality management systemNotified body: 1639Expiry: Apr 1, 2031
CN24/00005514Issued
Quality management systemNotified body: 1639Expiry: Aug 29, 2029
CN24/00005514Issued
Quality management systemNotified body: 1639Expiry: Aug 29, 2029
CN23/00003444Supplemented
Quality management systemNotified body: 1639Expiry: Jun 27, 2028

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

All products by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Market distribution

Primary placement in Germany; available across 32 countries total.

Country	On market since	Until
GermanyPrimary placement	Aug 5, 2015	Aug 5, 2065
Austria	Aug 5, 2015	Aug 5, 2065
Belgium	Aug 5, 2015	Aug 5, 2065
Bulgaria	Aug 5, 2015	Aug 5, 2065
Cyprus	Aug 5, 2015	Aug 5, 2065
Czechia	Aug 5, 2015	Aug 5, 2065
Denmark	Aug 5, 2015	Aug 5, 2065
Estonia	Aug 5, 2015	Aug 5, 2065
EL	Aug 5, 2015	Aug 5, 2065
Spain	Aug 5, 2015	Aug 5, 2065
Finland	Aug 5, 2015	Aug 5, 2065
France	Aug 5, 2015	Aug 5, 2065
Croatia	Aug 5, 2015	Aug 5, 2065
Hungary	Aug 5, 2015	Aug 5, 2065
Ireland	Aug 5, 2015	Aug 5, 2065
Iceland	Aug 5, 2015	Aug 5, 2065
Italy	Aug 5, 2015	Aug 5, 2065
Liechtenstein	Aug 5, 2015	Aug 5, 2065
Lithuania	Aug 5, 2015	Aug 5, 2065
Luxembourg	Aug 5, 2015	Aug 5, 2065
Latvia	Aug 5, 2015	Aug 5, 2065
Malta	Aug 5, 2015	Aug 5, 2065
Netherlands	Aug 5, 2015	Aug 5, 2065
Norway	Aug 5, 2015	Aug 5, 2065
Poland	Aug 5, 2015	Aug 5, 2065
Portugal	Aug 5, 2015	Aug 5, 2065
Romania	Aug 5, 2015	Aug 5, 2065
Sweden	Aug 5, 2015	Aug 5, 2065
Slovenia	Aug 5, 2015	Aug 5, 2065
Slovakia	Aug 5, 2015	Aug 5, 2065
Türkiye	Aug 5, 2015	Aug 5, 2065
XI	Aug 5, 2015	Aug 5, 2065

Temperature probe

Temperature probe

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates covering this device

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Related devices