EUDAMED last updated this device on May 11, 2026

STO126013P

805771755FT05FZ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BRM Extremities S.r.l.
UDI-DI code: 08057717556186
Reference / catalog number: STO126013P

STO126013P is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by BRM Extremities S.r.l.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on May 11, 2026

STO126013P

805771755FT05FZ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BRM Extremities S.r.l.
UDI-DI code: 08057717556186
Reference / catalog number: STO126013P

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 08057717556186
Basic UDI-DI: 805771755FT05FZ
Reference / catalog number: STO126013P
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://brm-extremities.com/
Clinical sizes: 13 MU50
2.6 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08057717556186

UDI-PI DataMatrix

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

EMDN nomenclature code(s)

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

P09120603CANNULATED SCREWS

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in Italy; available across 16 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
Austria		Still on market
Belgium		Still on market
Cyprus		Still on market
Germany		Still on market
Spain		Still on market
France		Still on market
Ireland		Still on market
Iceland		Still on market
Liechtenstein		Still on market
Luxembourg		Still on market
Malta		Still on market
Netherlands		Still on market
Poland		Still on market
Portugal		Still on market
XI		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08057717556186
Basic UDI-DI: 805771755FT05FZ
Reference / catalog number: STO126013P
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://brm-extremities.com/
Clinical sizes: 13 MU50
2.6 MU50

Manufacturer information

Organization name: BRM Extremities S.r.l.
SRN: IT-MF-000016087
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08057717556186

UDI-PI DataMatrix

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

EMDN nomenclature code(s)

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

P09120603CANNULATED SCREWS

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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

Certificates

Certificate health across this manufacturer's portfolio.

087-00-00-MDRIssued
Technical documentationNotified body: 0426Expiry: Dec 2, 2030
059-00-02-MDRSupplemented
Quality management systemNotified body: 0426Expiry: Sep 19, 2029
060-00-00-MDRWithdrawn
Quality management systemNotified body: 0426Expiry: Sep 19, 2029

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

All products by BRM Extremities S.r.l.

Market distribution

Primary placement in Italy; available across 16 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
Austria		Still on market
Belgium		Still on market
Cyprus		Still on market
Germany		Still on market
Spain		Still on market
France		Still on market
Ireland		Still on market
Iceland		Still on market
Liechtenstein		Still on market
Luxembourg		Still on market
Malta		Still on market
Netherlands		Still on market
Poland		Still on market
Portugal		Still on market
XI		Still on market

STO126013P

STO126013P

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates covering this device

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

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