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

38250021F — Class I MDR by Verreries Talançonnaises

MD Atlas
Verreries Talançonnaises

EUDAMED last updated this device on Apr 1, 2026

38250021F

0376039695-Cryokit-DS-RP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Verreries Talançonnaises
UDI-DI code: 03760396950064
Reference / catalog number: 38250021F

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: Verreries Talançonnaises
SRN: FR-MF-000019313
Manufacturer status: Active

Critical warnings

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

CW001
Produit déjà stérile, ne pas resterriliser
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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: not provided
UDI-DI code: 03760396950064
Basic UDI-DI: 0376039695-Cryokit-DS-RP
Reference / catalog number: 38250021F
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: Kit stérile pour le transport et le stockage de tissus d'origine humaine composé d'un sachet interne et d'un sachet externe.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A090199ORGAN COLLECTION CONTAINERS - 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

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.

Related devices

382500210376039695-Cryokit-DS-RPOn the market 38250034B0376039695-Cryokit-PS-TKOn the market 382500330376039695-Cryokit-PS-TKOn the market 382500350376039695-Cryokit-PS-TKOn the market 38250032B0376039695-Cryokit-PS-TKOn the market