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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

GPACK20 — Class I MDD by Hirondelle Medical

MD Atlas
Hirondelle Medical

EUDAMED last updated this device on Mar 28, 2022

GPACK20

B-37700244010738

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Hirondelle Medical
UDI-DI code: 37700244010738
Reference / catalog number: HDLM-GPACK20

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Manufacturer information

Organization name: Hirondelle Medical
SRN: FR-MF-000002432
Manufacturer status: Active

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Bouchon GDPB-37700244011100On the market BPACK100B-37700244010974On the market Broche de précisionB-37700244010288On the market Clé GDPB-37700244011032On the market EPACK20B-37700244010806On 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.

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: GPACK20
UDI-DI code: 37700244010738
Basic UDI-DI: B-37700244010738
Reference / catalog number: HDLM-GPACK20
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Conditionnement pour 20 guides de pose HM-GDP02
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L0922ORTHOPAEDIC SURGERY GUIDES, REUSABLE

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
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Software identification