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Organization name
UDI-DI code
Reference / catalog number

38250035 — Class I MDR by Verreries Talançonnaises

MD Atlas
Verreries Talançonnaises

EUDAMED last updated this device on Apr 1, 2026

38250035

0376039695-Cryokit-PS-TK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Verreries Talançonnaises
UDI-DI code: 03760396950132
Reference / catalog number: 38250035

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Manufacturer information

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

Related devices

382500210376039695-Cryokit-DS-RPOn the market 38250034B0376039695-Cryokit-PS-TKOn the market 382500330376039695-Cryokit-PS-TKOn the market 38250032B0376039695-Cryokit-PS-TKOn the market 382500310376039695-Cryokit-PS-TKOn 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

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

CW001
Produit déjà stérile, ne pas restériliser
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: 03760396950132
Basic UDI-DI: 0376039695-Cryokit-PS-TK
Reference / catalog number: 38250035
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 pot interne 350ml 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

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Software identification