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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

CER.10X5-20 — Class I MDR by D.R.M. S.R.L.

MD Atlas
D.R.M. S.R.L.

EUDAMED last updated this device on Jan 12, 2026

CER.10X5-20

805959152BCZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: D.R.M. S.R.L.
UDI-DI code: 08059591520512
Reference / catalog number: CER.10X5-20

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View device family (Basic UDI)

Manufacturer information

Organization name: D.R.M. S.R.L.
SRN: IT-MF-000027115
Manufacturer status: Active

Related devices

DR/ESP-2805959152APCPFOn the market DR/ESP-1805959152APCPFOn the market BANDAGE COHÉSIF POUR FISTULE805959152PREMN4On the market IB0786805959152PREMN4On the market DR 10-1A805959152PREMN4On the market

Certificates

Certificate health across this manufacturer's portfolio.

55998Reissued
Quality assuranceNotified body: 0546Expiry: Jan 24, 2028
55998Issued
Quality assuranceNotified body: 0546Expiry: Jan 24, 2028

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: 08059591520512
Basic UDI-DI: 805959152BCZ
Reference / catalog number: CER.10X5-20
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: 1 confezione da n. 20 cerotti cm 10x5
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: cm 5
cm 10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08059591520512

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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.

M050201EXTENSIBLE NON-WOVEN PLASTERS

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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