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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

30274 — Class IIa MDD by bitop AG

MD Atlas
bitop AG

EUDAMED last updated this device on Feb 9, 2026

30274

B-DE-MF-000006543-30274T7

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: bitop AG
UDI-DI code: D-DE-MF-000006543-30274T7
Reference / catalog number: 30274

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Manufacturer information

Organization name: bitop AG
SRN: DE-MF-000006543
Manufacturer status: Active

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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

1 warning recorded — scroll inside the panel to see all entries.

CW999
Children younger than 2 years should not use the product. The product should not be used in the case of hypersensitivity to Ectoin® or any of the other ingredients of the mouth and throat spray. If allergic reactions occur, the use of the product must be discontinued immediately. To ensure safe hygiene, each spray bottle should be used by one person only. Do not use for more than 3 months after opening. The product should be kept out of reach of children. Do not use if the device is damaged or punctured. If recommended by your doctor or health care professional, the product may be used after surgery and trauma. Safety of salvia and mint during pregnancy and while breast-feeding has not been established. In the absence of sufficient data, the use of the product during pregnancy and while breast-feeding is not recommended. Children and patients unable to use the product on their own should be assisted during application of the product.

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: D-DE-MF-000006543-30274T7
Basic UDI-DI: B-DE-MF-000006543-30274T7
Reference / catalog number: 30274
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC 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)

Q0399ENT DEVICES - 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