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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

LiNA SkinHook — Class IIa MDR by LiNA Medical AG

MD Atlas
LiNA Medical AG

EUDAMED last updated this device on Feb 25, 2026

LiNA SkinHook

57082651019-22D

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LiNA Medical AG
UDI-DI code: 05708265017225
Reference / catalog number: SH-120

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Manufacturer information

Organization name: LiNA Medical AG
SRN: CH-MF-000046832
Manufacturer status: Active

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Critical warnings

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

CW029
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW009
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.
CW032
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Denmark; available across 1 country total.

Country	On market since	Until
DenmarkPrimary placement		Still on market

Device identification

Trade name: LiNA SkinHook
UDI-DI code: 05708265017225
Basic UDI-DI: 57082651019-22D
Reference / catalog number: SH-120
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: The LiNA Skin Hook™ is together with LiNA SeaStar™ a complete system for retracting delicate soft tissue. By securing the LiNA Skin Hook™ on to the LiNA SeaStar™ the exposure of the incision is increased. The flexible and elastic hook can be adjusted during the procedure to create optimum tension. The LiNA Skin Hook™ is available with 4 different stainless steel hooks.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12019099VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

TNP/MDR/0050/5851/2026Issued
Quality management systemNotified body: 2274Expiry: Feb 19, 2031