EUDAMED last updated this device on May 27, 2026

Anesthesia Mask

B-06946430421838

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Xiamen Compower Medical Tech. Co., Ltd.
UDI-DI code: 06946430421838
Reference / catalog number: /

Anesthesia Mask is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Xiamen Compower Medical Tech. Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

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EUDAMED last updated this device on May 27, 2026

Anesthesia Mask

B-06946430421838

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Xiamen Compower Medical Tech. Co., Ltd.
UDI-DI code: 06946430421838
Reference / catalog number: /

View device family (Basic UDI)

Device identification

Trade name: Anesthesia Mask
UDI-DI code: 06946430421838
Basic UDI-DI: B-06946430421838
Reference / catalog number: /
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Anesthesia Mask is intended to be connected to the anesthesia machine through the breathing circuit, used to deliver anesthetic gases to the patient, and provide adjuvant treatment for the patient with respiratory failure.
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)06946430421838

EMDN nomenclature code(s)

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

R03010101ANAESTHETIC FACE MASKS

Critical warnings

No critical warnings reported for this device.

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	Oct 31, 2024	Still on market

Device identification

Trade name: Anesthesia Mask
UDI-DI code: 06946430421838
Basic UDI-DI: B-06946430421838
Reference / catalog number: /
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Anesthesia Mask is intended to be connected to the anesthesia machine through the breathing circuit, used to deliver anesthetic gases to the patient, and provide adjuvant treatment for the patient with respiratory failure.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Xiamen Compower Medical Tech. Co., Ltd.
SRN: CN-MF-000011703
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06946430421838

EMDN nomenclature code(s)

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

R03010101ANAESTHETIC FACE MASKS

Critical warnings

No critical warnings reported for this device.

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.

HZ 2375149-1Issued
Quality management systemNotified body: 0197Expiry: Oct 12, 2028

Legacy certificates

Certificate number: COMPO-PLA-2024-03-22
Type: MDD Annex V
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: Dec 31, 2028

Certificates covering this device

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

All products by Xiamen Compower Medical Tech. Co., Ltd.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Oct 31, 2024	Still on market

Anesthesia Mask

Anesthesia Mask

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI 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

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Legacy certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Legacy certificates

Related devices