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LiNA Xcise™, Laparoscopic Morcellator

FDA UDI

Class II (US FDA UDI)

by Lina Medical ApS

Identity

Trade Name
LiNA Xcise™, Laparoscopic Morcellator FDA UDI
Generic Name
Tissue morcellation system handpiece, battery-powered FDA UDI
Device Name
15mm battery powered morcellator system with obturator FDA UDI
Model / Reference
MOR-1515-1 FDA UDI
Description
15mm battery powered morcellator system with obturator FDA UDI

Identifiers

Catalog Number
MOR-1515-1 FDA UDI
Primary DI / UDI-DI
05708265013319 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Tissue morcellation system handpiece, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tissue morcellation system handpiece, battery-powered

LiNA Xcise™, Laparoscopic Morcellator by Lina Medical ApS — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue morcellation system handpiece, battery-powered.

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 0105b26e-21eb-45e7-ba24-4d389e67f9f7 34 fields · synced May 31, 2026