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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

IM-20 — Class I MDD by INORIS MEDICAL SP. Z O.O.

MD Atlas
INORIS MEDICAL SP. Z O.O.

EUDAMED last updated this device on Oct 7, 2022

IM-20

B-05902596226121

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: INORIS MEDICAL SP. Z O.O.
UDI-DI code: 05902596226121
Reference / catalog number: IM-20

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View device family (Basic UDI)

Manufacturer information

Organization name: INORIS MEDICAL SP. Z O.O.
SRN: PL-MF-000016864
Manufacturer status: Active

Related devices

IM-01B-05902596226015On the market IM-02B-05902596226091On the market IM-1080B-05902596226688On the market IM-40B-05902596226244On the market IM-45B-05902596226275On the market

Certificates

Certificate health across this manufacturer's portfolio.

1434-MDR-007/2026Issued
Quality management systemNotified body: 1434Expiry: Apr 2, 2031

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Poland; available across 1 country total.

Placed on the market in Poland; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05902596226121
Basic UDI-DI: B-05902596226121
Reference / catalog number: IM-20
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: Semi-open Clip-On Biteguard for adults is designed to protect both patient and the equipment during medical instrumentation. Due to its U shape it can be easily applied even when the instrument is in patient's mouth. Its optimal position is when the outside wings are placed between lips and teeth. It ensures that biteguard stays in correct position for the entire procedure. Clip-On Biteguard secures both patient and the instrument. It is designed to be used during gastroscopy, bronchoscopy and transesophageal echocardiography.
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.

G030804GASTROINTESTINAL ENDOSCOPY AND ECHOENDOSCOPY, BITE BLOCKS

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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