Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

H0.7GFT1.7L20D — Class IIb MDR by Newclip Technics SAS

MD Atlas
Newclip Technics SAS

EUDAMED last updated this device on May 7, 2026

H0.7GFT1.7L20D

37005696002794

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Newclip Technics SAS
UDI-DI code: 03700569672614
Reference / catalog number: H0.7GFT1.7L20D

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

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.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Mar 16, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03700569672614
Basic UDI-DI: 37005696002794
Reference / catalog number: H0.7GFT1.7L20D
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.

EMDN nomenclature code(s)

P09120603CANNULATED SCREWS

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

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

Related devices

Medial opening HTO plate - Right - Size 13700569600248WOn the market H1.1GFT2.6L14-ST37005696002794On the market H0.9IFT2.25L1637005696002794On the market H0.9IFT2.25L14-ST37005696002794On the market H0.9HFT2.25L1837005696002794

On the market