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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

3770031579048 — Class I MDR by Butterfly Therapeutics

MD Atlas
Butterfly Therapeutics

EUDAMED last updated this device on Oct 15, 2024

3770031579048

3770031579BlissDTX9Y

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Butterfly Therapeutics
UDI-DI code: 03770031579048
Reference / catalog number: 3770031579048

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Manufacturer information

Organization name: Butterfly Therapeutics
SRN: FR-MF-000036923
Manufacturer status: Inactive

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: not provided
UDI-DI code: 03770031579048
Basic UDI-DI: 3770031579BlissDTX9Y
Reference / catalog number: 3770031579048
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: Bliss One Pré installé sur casque Pico G2
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

Related devices

037700315790313770031579BlissDTX9YOn the market 037700315790243770031579BlissDTX9YOn 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.