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

CRYOSTAB PACK GENOU — Class I MDR by GROUPE SOBER SAS

MD Atlas
GROUPE SOBER SAS

EUDAMED last updated this device on May 27, 2024

CRYOSTAB PACK GENOU

37014598TECCRY004STKZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GROUPE SOBER SAS
UDI-DI code: 03701459810789
Reference / catalog number: CRYOSTAB PACK GENOU

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: GROUPE SOBER SAS
SRN: FR-MF-000017818
Manufacturer status: Active

Related devices

AMBI PLATEFORM37014598POIIMM031STRQOn the market ACCESSOIRE RIVETAGE LIBERTY37014598TECATM022STF5On the market CHEVILLE TECHNOCONCEPT37014598TECHCO005C17GOn the market CML CRYOSTAB37014598LOMCRY001STU2On the market CML CRYOSTAB37014598LOMCRY001STU2On 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.

Critical warnings

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

CW018
Consulter les précautions d’emploi et méthode de pose avant utilisation.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: CRYOSTAB PACK GENOU
UDI-DI code: 03701459810789
Basic UDI-DI: 37014598TECCRY004STKZ
Reference / catalog number: CRYOSTAB PACK GENOU
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: Les compresses CryoStab® ne brûlent pas et ne blessent pas les tissus cutanés. Les compresses CryoStab® sont non toxiques et ne sont pas destinées à un usage interne.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 14X14 & 14X28

EMDN nomenclature code(s)

M030504IMMOBILISATION SYSTEMS, MOULDABLE UNDER COLD AND HOT TEMPRATURES

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