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LiNA Skin Hook™

FDA UDI

Class I (US FDA UDI)

by Lina Medical ApS

Identity

Trade Name
LiNA Skin Hook™ FDA UDI
Generic Name
Surgical retractor/retraction system blade, single-use FDA UDI
Device Name
SMALL BLUNT, dual pack FDA UDI
Model / Reference
SH-120 FDA UDI
Description
SMALL BLUNT, dual pack FDA UDI

Identifiers

Catalog Number
SH-120 FDA UDI
Primary DI / UDI-DI
05708265000418 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Surgical retractor/retraction system blade, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical retractor/retraction system blade, single-use

LiNA Skin Hook™ by Lina Medical ApS — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lina Medical ApS

Sources (1)

  • FDA UDI babb0ffb-3c0b-40c2-b7cc-8b4207787982 35 fields · synced Jun 1, 2026