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

Hook to pull the loop — Class I MDD by movmedix

MD Atlas
movmedix

EUDAMED last updated this device on May 20, 2026

Hook to pull the loop

B-03700435646664

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: movmedix
UDI-DI code: 03700435646664
Reference / catalog number: D21042

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: movmedix
SRN: FR-MF-000000914
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

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	Jan 1, 2011	Still on market

Device identification

Trade name: Hook to pull the loop
UDI-DI code: 03700435646664
Basic UDI-DI: B-03700435646664
Reference / catalog number: D21042
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC 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: Handle — 120 MU50
Hook — 175 MU50

EMDN nomenclature code(s)

L0999ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER

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

Related devices

7.5 mm reduction for curved wire-passer cannulaB-03700435646039On the market ACPL03 BodyB-03700435635439On the market ACPL03 HandleB-03700435635446On the market Acromio-clavicular guideB-03700435630595On the market Adjustable guideB-03700435630489

On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.