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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

BPCD18L — Class I MDR by SCHILLER AG

MD Atlas
SCHILLER AG

EUDAMED last updated this device on May 5, 2026

BPCD18L

761336500000000452

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SCHILLER AG
UDI-DI code: 07613365003420
Reference / catalog number: 2.120082

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Manufacturer information

Organization name: SCHILLER AG
SRN: CH-MF-000012722
Manufacturer status: Active

Related devices

PB-3000 Var. 476133650000000014UOn the market PB-3000 Var. 7, sub-variant: C (main device 3.921008)76133650000000014UOn the market ARGUS LifePoint761336500000001659On the market ARGUS LifePoint 2761336500000001659On the market ARGUS PB-1000B-07613365000092On the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: BPCD18L
UDI-DI code: 07613365003420
Basic UDI-DI: 761336500000000452
Reference / catalog number: 2.120082
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: SCHILLER AG NIBP cuffs are accessories used in conjunction with SCHILLER AG noninvasive blood pressure (NIBP) measurement base units. Systolic and diastolic arterial blood pressure at the level of the brachial artery as well as heart rate are measured in an automated fashion, and measurements are performed via an oscillometric measurement technique or an auscultatory method.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z1203020302NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS

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

Certificates

Certificate health across this manufacturer's portfolio.

G10 041505 0132Issued
Quality management systemNotified body: 0123Expiry: Nov 11, 2026