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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

Bambi Belt Size 1 — Class I MDR by Bambi Belt B.V.

MD Atlas
Bambi Belt B.V.

EUDAMED last updated this device on Mar 24, 2026

Bambi Belt Size 1

8720256769BELT01AV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bambi Belt B.V.
UDI-DI code: 87202567690154
Reference / catalog number: BELT-N01.1

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View device family (Basic UDI)

Manufacturer information

Organization name: Bambi Belt B.V.
SRN: NL-MF-000010914
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW027
EUDAMED did not publish a description for this code.
CW999
is not intended for: • Use during Electrosurgery. • Home use. • Ambulatory use.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Dec 1, 2023	Still on market

Device identification

Trade name: Bambi Belt Size 1
UDI-DI code: 87202567690154
Basic UDI-DI: 8720256769BELT01AV
Reference / catalog number: BELT-N01.1
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: 10
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: -1–1 MU29

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)87202567690154

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Z1203020285MULTI-PARAMETER MONITORS - CONSUMABLES

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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Certificates

Certificate health across this manufacturer's portfolio.

10000468205-PA-NoMA-CZEIssued
Quality management systemNotified body: 2460Expiry: May 9, 2028