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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

BATLP2A3F2PT2 — Class I MDR by B&D Bracci e…

MD Atlas
B&D Bracci e dispositivi s.r.l.

EUDAMED last updated this device on Jun 9, 2025

BATLP2A3F2PT2

805750259BATJY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: B&D Bracci e dispositivi s.r.l.
UDI-DI code: 08057502590227
Reference / catalog number: BATLP2A3F2PT2

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View device family (Basic UDI)

Manufacturer information

Organization name: B&D Bracci e dispositivi s.r.l.
SRN: IT-MF-000015845
Manufacturer status: Active

Related devices

BLGA000040805750259BLCJXOn the market BATLP2A3F1PT5805750259BATJYOn the market APLM00001805750259APLM000000BGOn the market APLP00001805750259APLP170060GFOn the market APPSO0001805750259APPSO130060JTOn the market

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

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08057502590227
Basic UDI-DI: 805750259BATJY
Reference / catalog number: BATLP2A3F2PT2
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: ARTICULATED ARM FOR LINEAR CAMERA WALL (FIXED 600MM + ARTICULATED 900MM + EXTENSION 150MM)
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

UDI-DI DataMatrix

Encoded

(01)08057502590227

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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.

V0899MEDICAL SUPPORT EQUIPMENT - 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

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