EUDAMED last updated this device on May 26, 2026

Verifine

697122740IPNPZ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Promisemed Hangzhou Meditech Co., Ltd.
UDI-DI code: 06975965293757
Reference / catalog number: NPN-32*6Q

Verifine is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Promisemed Hangzhou Meditech Co., Ltd.. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on May 26, 2026

Verifine

697122740IPNPZ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Promisemed Hangzhou Meditech Co., Ltd.
UDI-DI code: 06975965293757
Reference / catalog number: NPN-32*6Q

View device family (Basic UDI)

Device identification

Trade name: Verifine
UDI-DI code: 06975965293757
Basic UDI-DI: 697122740IPNPZ
Reference / catalog number: NPN-32*6Q
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: 50
Additional product description: This product is used in conjunction with an injection pen for subcutaneous drug administration.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 6mm
32G

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06975965293757

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.

A0101010202HYPODERMIC PEN NEEDLES, W/O SAFETY SYSTEMS

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW030
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
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 EL; available across 1 country total.

Country	On market since	Until
ELPrimary placement		Still on market

Device identification

Trade name: Verifine
UDI-DI code: 06975965293757
Basic UDI-DI: 697122740IPNPZ
Reference / catalog number: NPN-32*6Q
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: 50
Additional product description: This product is used in conjunction with an injection pen for subcutaneous drug administration.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 6mm
32G

Manufacturer information

Organization name: Promisemed Hangzhou Meditech Co., Ltd.
SRN: CN-MF-000008465
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06975965293757

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.

A0101010202HYPODERMIC PEN NEEDLES, W/O SAFETY SYSTEMS

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW030
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
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.

HZ 2091024-1Supplemented
Quality management systemNotified body: 0197Expiry: Nov 13, 2030
HZ 2091024-1Supplemented
Quality management systemNotified body: 0197Expiry: Nov 13, 2025

Certificates covering this device

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

All products by Promisemed Hangzhou Meditech Co., Ltd.

Market distribution

Primary placement in EL; available across 1 country total.

Country	On market since	Until
ELPrimary placement		Still on market

Verifine

Verifine

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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