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

HIPUPAXR — Class I MDR by MEDIDEV - SENTECH FRANCE

MD Atlas
MEDIDEV - SENTECH FRANCE

EUDAMED last updated this device on Apr 27, 2026

HIPUPAXR

376033037HIPUPA1GD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDIDEV - SENTECH FRANCE
UDI-DI code: 03760330371276
Reference / catalog number: HIPUPAXR

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: MEDIDEV - SENTECH FRANCE
SRN: FR-MF-000008021
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760330371276
Basic UDI-DI: 376033037HIPUPA1GD
Reference / catalog number: HIPUPAXR
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: Housse SENTRY 1200 ST partie supérieure matelassée total move 90 x 200
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T030502BED AND STRETCHER HYGIENIC COVERS

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

C1200C014550376033037C1200C1DSOn the market HIC4550376033037HIC16XOn the market HIPUPA376033037HIPUPA1GDOn the market HIPUPA120200376033037HIPUPA1GDOn the market M1200MR02376033037M1200MR1PXOn 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.