EUDAMED last updated this device on May 26, 2026

Ventilator

697081942RS300KU

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Resvent Medical Technology Co., Ltd.
UDI-DI code: 06970819423410
Reference / catalog number: RS100

Ventilator is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Resvent Medical Technology Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

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Country
Date of registration
Address

EUDAMED last updated this device on May 26, 2026

Ventilator

697081942RS300KU

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Resvent Medical Technology Co., Ltd.
UDI-DI code: 06970819423410
Reference / catalog number: RS100

View device family (Basic UDI)

Device identification

Trade name: Ventilator
UDI-DI code: 06970819423410
Basic UDI-DI: 697081942RS300KU
Reference / catalog number: RS100
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: The device is intended to provide temporary or long-term invasive or non-invasive mechanical ventilation for adult, paediatric, or infant patients.
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)06970819423410

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.

Z1203010504ADULT AND PAEDIATRIC/NEONATAL PULMONARY VENTILATORS

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: Ventilator
UDI-DI code: 06970819423410
Basic UDI-DI: 697081942RS300KU
Reference / catalog number: RS100
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: The device is intended to provide temporary or long-term invasive or non-invasive mechanical ventilation for adult, paediatric, or infant patients.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Resvent Medical Technology Co., Ltd.
SRN: CN-MF-000012608
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06970819423410

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.

Z1203010504ADULT AND PAEDIATRIC/NEONATAL PULMONARY VENTILATORS

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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.

G15 096632 0018Reissued
Quality management systemNotified body: 0123Expiry: Oct 23, 2029

Certificates covering this device

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

All products by Resvent Medical Technology Co., Ltd.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Ventilator

Ventilator

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

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