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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

AG28-0002 — Class I MDR by X.NOV MEDICAL TECHNOLOGY

MD Atlas
X.NOV MEDICAL TECHNOLOGY

EUDAMED last updated this device on May 28, 2026

AG28-0002

3700535100014PQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: X.NOV MEDICAL TECHNOLOGY
UDI-DI code: 03700535160879
Reference / catalog number: AG28-0002

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View device family (Basic UDI)

Manufacturer information

Organization name: X.NOV MEDICAL TECHNOLOGY
SRN: CH-MF-000018319
Manufacturer status: Active

Related devices

AG02-00033700535100054Q4On the market AG03-12353700535100054Q4On the market AG03-08443700535100054Q4On the market AG02-00133700535100054Q4On the market AG02-40123700535100054Q4On 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 France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Mar 27, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03700535160879
Basic UDI-DI: 3700535100014PQ
Reference / catalog number: AG28-0002
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: —
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)03700535160879

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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.

L0922ORTHOPAEDIC SURGERY GUIDES, REUSABLE

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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