EUDAMED last updated this device on Apr 22, 2026

H1.1HFT2.6L30

37005696002794

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Newclip Technics SAS
UDI-DI code: 03700569618018
Reference / catalog number: H1.1HFT2.6L30

View device family (Basic UDI)

Role
Country
Date of registration
Address

EUDAMED last updated this device on Apr 22, 2026

H1.1HFT2.6L30

37005696002794

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Newclip Technics SAS
UDI-DI code: 03700569618018
Reference / catalog number: H1.1HFT2.6L30

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 03700569618018
Basic UDI-DI: 37005696002794
Reference / catalog number: H1.1HFT2.6L30
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: —
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)03700569618018

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.

P09120603CANNULATED SCREWS

Critical warnings

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

CW007
EUDAMED did not publish a description for this code.
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 France; available across 9 countries total.

Country	On market since	Until
FrancePrimary placement	Sep 14, 2022	Still on market
Belgium	Sep 14, 2022	Still on market
Germany	Sep 14, 2022	Still on market
EL	Sep 14, 2022	Still on market
Spain	Sep 14, 2022	Still on market
Finland	Sep 14, 2022	Still on market
Italy	Sep 14, 2022	Still on market
Portugal	Sep 14, 2022	Still on market
Romania	Sep 14, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03700569618018
Basic UDI-DI: 37005696002794
Reference / catalog number: H1.1HFT2.6L30
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Newclip Technics SAS
SRN: FR-MF-000011809
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)03700569618018

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.

P09120603CANNULATED SCREWS

Critical warnings

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

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

FR22/00000038Supplemented
Quality management systemNotified body: 1639Expiry: Sep 13, 2027

Certificates covering this device

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

Market distribution

Primary placement in France; available across 9 countries total.

Country	On market since	Until
FrancePrimary placement	Sep 14, 2022	Still on market
Belgium	Sep 14, 2022	Still on market
Germany	Sep 14, 2022	Still on market
EL	Sep 14, 2022	Still on market
Spain	Sep 14, 2022	Still on market
Finland	Sep 14, 2022	Still on market
Italy	Sep 14, 2022	Still on market
Portugal	Sep 14, 2022	Still on market
Romania	Sep 14, 2022	Still on market

H1.1HFT2.6L30

H1.1HFT2.6L30

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