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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

6005.7 — Class I MDR by LABORATORIOS HERBITAS,…

MD Atlas
LABORATORIOS HERBITAS, S.L.

EUDAMED last updated this device on May 4, 2026

6005.7

84351355DUPLIGEL7U

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATORIOS HERBITAS, S.L.
UDI-DI code: 08435135523230
Reference / catalog number: 6005.7

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Manufacturer information

Organization name: LABORATORIOS HERBITAS, S.L.
SRN: ES-MF-000004599
Manufacturer status: Active

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10.025.384351355BLANDAGJOn the market 10.025.184351355BLANDAGJOn the market 10.025.484351355BLANDAGJOn the market 6073.384351355DUPLOQ9On the market 6073.284351355DUPLOQ9On 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 Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08435135523230
Basic UDI-DI: 84351355DUPLIGEL7U
Reference / catalog number: 6005.7
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y99DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - 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
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Software identification