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

0148 — Class I MDR by Implants Diffusion…

MD Atlas
Implants Diffusion International

EUDAMED last updated this device on Apr 12, 2022

0148

03662174REUINSTRX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Implants Diffusion International
UDI-DI code: 03662174006072
Reference / catalog number: 0148

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: Implants Diffusion International
SRN: FR-MF-000000597
Manufacturer status: Active

Related devices

000403662174REUINSTRXOn the market 001403662174REUINSTRXOn the market 001603662174REUINSTRXOn the market 002503662174INSTRUL2On the market 003603662174REUINSTRXOn the market

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: 0148
UDI-DI code: 03662174006072
Basic UDI-DI: 03662174REUINSTRX
Reference / catalog number: 0148
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Abutment remover M2, L 34 mm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L0399GENERAL 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

Certificates

Certificate health across this manufacturer's portfolio.

FR25/00000112Issued
Quality management systemNotified body: 1639Expiry: May 12, 2030