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Organization name
UDI-DI code
Reference / catalog number

GC17C (bottle 200 mL) — Class IIa MDD by S.I.I.T. srl

MD Atlas
S.I.I.T. srl

EUDAMED last updated this device on May 22, 2026

GC17C (bottle 200 mL)

B-060070466V

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: S.I.I.T. srl
UDI-DI code: D-060070466V
Reference / catalog number: GC17C (bottle 200 mL)

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View device family (Basic UDI)

Manufacturer information

Organization name: S.I.I.T. srl
SRN: IT-MF-000022188
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

065-00-01-MDRSupplemented
Quality management systemNotified body: 0426Expiry: Nov 20, 2029

Critical warnings

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

CW010
.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-060070466V
Basic UDI-DI: B-060070466V
Reference / catalog number: GC17C (bottle 200 mL)
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: Medical device useful to treat or prevent gastroesophageal reflux and gastric hyperacidity, as well as to protect the mucosal tissues of stomach and esophagus from the potential damage caused by these conditions.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

G0401ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS

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

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