EUDAMED last updated this device on May 22, 2026

CCMED

697507091CNZN

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ShenZhen Bi-rich Medical Devices Co., Ltd
UDI-DI code: 06975070916282
Reference / catalog number: BR-CN136

CCMED is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by ShenZhen Bi-rich Medical Devices Co., Ltd. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

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Country
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EUDAMED last updated this device on May 22, 2026

CCMED

697507091CNZN

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ShenZhen Bi-rich Medical Devices Co., Ltd
UDI-DI code: 06975070916282
Reference / catalog number: BR-CN136

View device family (Basic UDI)

Device identification

Trade name: CCMED
UDI-DI code: 06975070916282
Basic UDI-DI: 697507091CNZN
Reference / catalog number: BR-CN136
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: This product is designed to deliver the prescribed medication solution to treat patient respiratory disorders. The nebulizer converts the medication solution into an aerosolized mist which is inhaled by the patient through the mouthpiece or mask.
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)06975070916282

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.

R060101COLD NEBULISATION SYSTEMS

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

Market distribution

Primary placement in Türkiye; available across 1 country total.

Country	On market since	Until
TürkiyePrimary placement	Sep 26, 2025	Still on market

Device identification

Trade name: CCMED
UDI-DI code: 06975070916282
Basic UDI-DI: 697507091CNZN
Reference / catalog number: BR-CN136
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: This product is designed to deliver the prescribed medication solution to treat patient respiratory disorders. The nebulizer converts the medication solution into an aerosolized mist which is inhaled by the patient through the mouthpiece or mask.
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 Bi-rich Medical Devices Co., Ltd
SRN: CN-MF-000023061
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06975070916282

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.

R060101COLD NEBULISATION SYSTEMS

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.

FI25/1008018Issued
Quality management systemNotified body: 0598Expiry: Nov 4, 2030
CN25/00003166Issued
Quality management systemNotified body: 1639Expiry: May 15, 2030

Legacy certificates

Certificate number: CN25/00003166
Type: Quality management system
Notified body: SGS Belgium NV (1639)
Validity: May 15, 2025 → May 15, 2030

Certificates covering this device

CN25/00003166Issued
Quality management systemNotified body: 1639Expiry: May 15, 2030

All products by ShenZhen Bi-rich Medical Devices Co., Ltd

Market distribution

Primary placement in Türkiye; available across 1 country total.

Country	On market since	Until
TürkiyePrimary placement	Sep 26, 2025	Still on market

CCMED

CCMED

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

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

Legacy certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Legacy certificates

Certificates covering this device

Related devices