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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

Coalgan Poudre — Class IIa MDR by Les Laboratoires BROTHIER

MD Atlas
Les Laboratoires BROTHIER

EUDAMED last updated this device on Dec 19, 2024

Coalgan Poudre

37003272COSHPOUDREW5

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Les Laboratoires BROTHIER
UDI-DI code: 03700327200196
Reference / catalog number: 0019

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Manufacturer information

Organization name: Les Laboratoires BROTHIER
SRN: FR-MF-000004023
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Dec 19, 2024	Still on market

Device identification

Trade name: Coalgan Poudre
UDI-DI code: 03700327200196
Basic UDI-DI: 37003272COSHPOUDREW5
Reference / catalog number: 0019
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M04040201ALGINATE DRESSINGS, NON-COMBINED

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

This device is not currently linked to any other device.

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.