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

MOLLETIERE SKINTAPE T5 — Class I MDR by Orliman, S.L.U.

MD Atlas
Orliman, S.L.U.

EUDAMED last updated this device on May 19, 2026

MOLLETIERE SKINTAPE T5

84350259ORLSM204124H

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Orliman, S.L.U.
UDI-DI code: 08435025929654
Reference / catalog number: JA06BI5

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: Orliman, S.L.U.
SRN: ES-MF-000001598
Manufacturer status: Active

Related devices

ANNEAU CLAVICULAIRE T1 / PÉDIATRIQUE84350259ORLSM203114AOn the market ANNEAU CLAVICULAIRE T2 / ENFANT84350259ORLSM203114AOn the market ANNEAU CLAVICULAIRE T384350259ORLSM203114AOn the market ANNEAU CLAVICULAIRE T484350259ORLSM203114AOn the market ANNEAU CLAVICULAIRE T584350259ORLSM203114AOn 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.

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: MOLLETIERE SKINTAPE T5
UDI-DI code: 08435025929654
Basic UDI-DI: 84350259ORLSM204124H
Reference / catalog number: JA06BI5
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: https://www.orliman.fr/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y061299LOWER EXTREMITY ORTHOSES - 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