EUDAMED last updated this device on Aug 12, 2025

BF24.10

805715896TF05HF

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medicap S.r.l
UDI-DI code: 08057158962898
Reference / catalog number: BF24.10

BF24.10 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Medicap 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 Aug 12, 2025

BF24.10

805715896TF05HF

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medicap S.r.l
UDI-DI code: 08057158962898
Reference / catalog number: BF24.10

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 08057158962898
Basic UDI-DI: 805715896TF05HF
Reference / catalog number: BF24.10
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: 100
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)08057158962898

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.

P9099IMPLANTABLE PROSTHETIC DEVICES - OTHER

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW010
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

Market distribution

Primary placement in Italy; available across 21 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
Austria		Still on market
Belgium		Still on market
Bulgaria		Still on market
Cyprus		Still on market
Czechia		Still on market
Germany		Still on market
Denmark		Still on market
EL		Still on market
Spain		Still on market
France		Still on market
Croatia		Still on market
Hungary		Still on market
Netherlands		Still on market
Norway		Still on market
Poland		Still on market
Portugal		Still on market
Romania		Still on market
Sweden		Still on market
Türkiye		Still on market
XI		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08057158962898
Basic UDI-DI: 805715896TF05HF
Reference / catalog number: BF24.10
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: 100
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Medicap S.r.l
SRN: IT-MF-000007995
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08057158962898

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.

P9099IMPLANTABLE PROSTHETIC DEVICES - OTHER

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW010
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.

CSQ0002220223Supplemented
Quality management systemNotified body: 0373Expiry: Dec 22, 2027
CVD000122Issued
Technical documentationNotified body: 0373Expiry: Dec 22, 2027

Legacy certificates

Certificate number: CSQ0002220223
Type: Quality management system
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Feb 9, 2023 → Dec 22, 2027

Certificate number: CVD000122
Type: Technical documentation
Notified body: ISTITUTO SUPERIORE DI SANITA' (0373)
Validity: Dec 23, 2022 → Dec 22, 2027

Certificates covering this device

All products by Medicap S.r.l

Market distribution

Primary placement in Italy; available across 21 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
Austria		Still on market
Belgium		Still on market
Bulgaria		Still on market
Cyprus		Still on market
Czechia		Still on market
Germany		Still on market
Denmark		Still on market
EL		Still on market
Spain		Still on market
France		Still on market
Croatia		Still on market
Hungary		Still on market
Netherlands		Still on market
Norway		Still on market
Poland		Still on market
Portugal		Still on market
Romania		Still on market
Sweden		Still on market
Türkiye		Still on market
XI		Still on market

BF24.10

BF24.10

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

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

Legacy certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Legacy certificates

Certificates covering this device

Related devices