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

GENUGIB POSTOP — Class I MDR by GIBAUD

MD Atlas
GIBAUD

EUDAMED last updated this device on Jan 13, 2026

GENUGIB POSTOP

332254046KW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GIBAUD
UDI-DI code: 03322544706130
Reference / catalog number: 6498-1

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: GIBAUD
SRN: FR-MF-000014279
Manufacturer status: Active

Related devices

GELA NOIR T35332254057L3On the market GELA NOIR T36332254057L3On the market GELA NOIR T37332254057L3On the market GELA NOIR T38332254057L3On the market GELA NOIR T39332254057L3On the market

Critical warnings

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

CW030
Consult healthcare professional before use
CW010
Consult instructions for use
CW011
Caution

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: GENUGIB POSTOP
UDI-DI code: 03322544706130
Basic UDI-DI: 332254046KW
Reference / catalog number: 6498-1
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y061209KNEE ORTHOSES

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

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.